Christine M. Hall, Ph.D. - Publications

Affiliations: 
2004 Emory University, Atlanta, GA 
Area:
developmental psychopathology

97 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Hall C, Jones S. Making sense in the city: Dolly Parton, early reading and educational policy-making Literacy. 50: 40-48. DOI: 10.1111/lit.12069  0.8
2016 Hall C, Thomson P. Creativity in teaching: what can teachers learn from artists? Research Papers in Education. 1-15. DOI: 10.1080/02671522.2016.1144216  0.8
2015 Bonafe L, Cormier-Daire V, Hall C, Lachman R, Mortier G, Mundlos S, Nishimura G, Sangiorgi L, Savarirayan R, Sillence D, Spranger J, Superti-Furga A, Warman M, Unger S. Nosology and classification of genetic skeletal disorders: 2015 revision. American Journal of Medical Genetics. Part A. PMID 26394607 DOI: 10.1002/ajmg.a.37365  0.8
2015 Rossi M, Hall CM, Bouvier R, Collardeau-Frachon S, Le Breton F, Bucourt M, Cordier MP, Vianey-Saban C, Parenti G, Andria G, Le Merrer M, Edery P, Offiah AC. Radiographic features of the skeleton in disorders of post-squalene cholesterol biosynthesis. Pediatric Radiology. 45: 965-76. PMID 25646736 DOI: 10.1007/s00247-014-3257-9  0.8
2015 Thomson P, Hall C. ‘Everyone can imagine their own Gellert’: the democratic artist and ‘inclusion’ in primary and nursery classrooms Education 3-13. 43: 420-432. DOI: 10.1080/03004279.2015.1020660  0.8
2015 Thomson P, Barrett A, Hall C, Hanby J, Jones S. Arts in the community as a place-making event The Routledge International Handbook of the Arts and Education. 295-304.  0.8
2014 Mitsui T, Kim OH, Hall CM, Offiah A, Johnson D, Jin DK, Toh TH, Soneda S, Keino D, Matsubayashi S, Ishii T, Nishimura G, Hasegawa T. Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2. American Journal of Medical Genetics. Part A. 164: 2529-34. PMID 25044890 DOI: 10.1002/ajmg.a.36669  0.8
2014 Mamais A, Chia R, Beilina A, Hauser DN, Hall C, Lewis PA, Cookson MR, Bandopadhyay R. Arsenite stress down-regulates phosphorylation and 14-3-3 binding of leucine-rich repeat kinase 2 (LRRK2), promoting self-association and cellular redistribution. The Journal of Biological Chemistry. 289: 21386-400. PMID 24942733 DOI: 10.1074/jbc.M113.528463  0.8
2014 Kumar V, Everingham S, Hall C, Greer PA, Craig AW. Calpains promote neutrophil recruitment and bacterial clearance in an acute bacterial peritonitis model. European Journal of Immunology. 44: 831-41. PMID 24375267 DOI: 10.1002/eji.201343757  0.8
2014 Franks A, Thomson P, Hall C, Jones K. Teachers, Arts Practice and Pedagogy Changing English: Studies in Culture and Education. 21: 171-181. DOI: 10.1080/1358684X.2014.897042  0.8
2013 Thomson P, Hall C, Jones K. Towards educational change leadership as a discursive practice-or should all school leaders read Foucault? International Journal of Leadership in Education. 16: 155-172. DOI: 10.1080/13603124.2012.693204  0.8
2013 Jones S, Hall C, Thomson P, Barrett A, Hanby J. Re-presenting the 'forgotten estate': Participatory theatre, place and community identity Discourse. 34: 118-131. DOI: 10.1080/01596306.2012.704686  0.8
2012 Mansour S, Swinkels M, Terhal PA, Wilson LC, Rich P, Van Maldergem L, Zwijnenburg PJ, Hall CM, Robertson SP, Newbury-Ecob R. Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance. European Journal of Human Genetics : Ejhg. 20: 1024-31. PMID 22473091 DOI: 10.1038/ejhg.2012.57  0.8
2012 Jackson GC, Mittaz-Crettol L, Taylor JA, Mortier GR, Spranger J, Zabel B, Le Merrer M, Cormier-Daire V, Hall CM, Offiah A, Wright MJ, Savarirayan R, Nishimura G, Ramsden SC, Elles R, et al. Pseudoachondroplasia and multiple epiphyseal dysplasia: a 7-year comprehensive analysis of the known disease genes identify novel and recurrent mutations and provides an accurate assessment of their relative contribution. Human Mutation. 33: 144-57. PMID 21922596 DOI: 10.1002/humu.21611  0.8
2012 Thomson P, Hall C, Jones K. Creativity and cross-curriculum strategies in England: Tales of doing, forgetting and not knowing International Journal of Educational Research. 55: 6-15. DOI: 10.1016/j.ijer.2012.06.003  0.8
2011 Boyden ED, Campos-Xavier AB, Kalamajski S, Cameron TL, Suarez P, Tanackovic G, Tanackovich G, Andria G, Ballhausen D, Briggs MD, Hartley C, Cohn DH, Davidson HR, Hall C, Ikegawa S, et al. Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity. American Journal of Human Genetics. 89: 767-72. PMID 22152678 DOI: 10.1016/j.ajhg.2011.12.012  0.8
2011 Parker MJ, Deshpande C, Rankin J, Wilson LC, Balasubramanian M, Hall CM, Wagner BE, Pollitt R, Dalton A, Bishop NJ. Type 1 collagenopathy presenting with a Russell-Silver phenotype. American Journal of Medical Genetics. Part A. 155: 1414-8. PMID 21567925 DOI: 10.1002/ajmg.a.33998  0.8
2011 Warman ML, Cormier-Daire V, Hall C, Krakow D, Lachman R, LeMerrer M, Mortier G, Mundlos S, Nishimura G, Rimoin DL, Robertson S, Savarirayan R, Sillence D, Spranger J, Unger S, et al. Nosology and classification of genetic skeletal disorders: 2010 revision. American Journal of Medical Genetics. Part A. 155: 943-68. PMID 21438135 DOI: 10.1002/ajmg.a.33909  0.8
2011 Goodman SH, Rouse MH, Connell AM, Broth MR, Hall CM, Heyward D. Maternal depression and child psychopathology: a meta-analytic review. Clinical Child and Family Psychology Review. 14: 1-27. PMID 21052833 DOI: 10.1007/s10567-010-0080-1  0.8
2011 Thomson P, Hall C. Sense-making as a lens on everyday change leadership practice: The case of Holly Tree Primary International Journal of Leadership in Education. 14: 385-403. DOI: 10.1080/13603124.2011.585665  0.8
2010 Collinson M, Leonard SJ, Charlton J, Crolla JA, Silve C, Hall CM, Oglivie C, James MA, Smithson SF. Symmetrical enchondromatosis is associated with duplication of 12p11.23 to 12p11.22 including PTHLH. American Journal of Medical Genetics. Part A. 152: 3124-8. PMID 21082660 DOI: 10.1002/ajmg.a.33567  0.8
2010 Race H, Hall CM, Harrison MG, Quarrell OW, Wakeling EL. A distinct autosomal recessive disorder of limb development with preaxial brachydactyly, phalangeal duplication, symphalangism and hyperphalangism. Clinical Dysmorphology. 19: 23-7. PMID 19952732 DOI: 10.1097/MCD.0b013e328334557e  0.8
2010 Lowe C, Subar D, Hall C, Kumpavat J, Decadt B, Agwunobi A. Hiatal hernias presenting as a late complication of laparoscopic-assisted cardio-oesophagectomy Hernia. 14: 211-213. PMID 19590816 DOI: 10.1007/s10029-009-0531-0  0.8
2010 Bishop N, Harrison R, Ahmed F, Shaw N, Eastell R, Campbell M, Knowles E, Hill C, Hall C, Chapman S, Sprigg A, Rigby A. A randomized, controlled dose-ranging study of risedronate in children with moderate and severe osteogenesis imperfecta. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 32-40. PMID 19580461 DOI: 10.1359/jbmr.090712  0.8
2010 Hall C, Thomson P. Grounded literacies: The power of listening to, telling and performing community stories Literacy. 44: 69-75. DOI: 10.1111/j.1741-4369.2010.00553.x  0.8
2010 Hall C. Creativity in recent educational discourse in England World Englishes. 29: 481-492. DOI: 10.1111/j.1467-971X.2010.01676.x  0.8
2010 Thomson P, Hall C, Jones K. Maggie's day: A small-scale analysis of English education policy Journal of Education Policy. 25: 639-656. DOI: 10.1080/02680931003783346  0.8
2009 Becker K, Howard K, Klazinga D, Hall CM. Caudal duplication syndrome with unilateral hypoplasia of the pelvis and lower limb and ventriculoseptal heart defect in a mother and features of VATER association in her child. Clinical Dysmorphology. 18: 139-41. PMID 19474703 DOI: 10.1097/MCD.0b013e32832d0703  0.8
2009 Smithson SF, Grier D, Hall CM. Spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type. Clinical Dysmorphology. 18: 31-5. PMID 19050402 DOI: 10.1097/MCD.0b013e3283189762  0.8
2009 Hall C, Noyes A. New regimes of truth: The impact of performative school self evaluation systems on teachers' professional identities Teaching and Teacher Education. 25: 850-856. DOI: 10.1016/j.tate.2009.01.008  0.8
2008 Goodman SH, Broth MR, Hall CM, Stowe ZN. Treatment of postpartum depression in mothers: Secondary benefits to the infants. Infant Mental Health Journal. 29: 492-513. PMID 28636221 DOI: 10.1002/imhj.20188  0.8
2008 Sousa SB, Russell-Eggitt I, Hall C, Hall BD, Hennekam RCM. Further delineation of spondylometaphyseal dysplasia with cone-rod dystrophy American Journal of Medical Genetics, Part A. 146: 3186-3194. PMID 19012331 DOI: 10.1002/ajmg.a.32576  0.8
2008 Irving MD, Chitty LS, Mansour S, Hall CM. Chondrodysplasia punctata: a clinical diagnostic and radiological review. Clinical Dysmorphology. 17: 229-41. PMID 18978650 DOI: 10.1097/MCD.0b013e3282fdcc70  0.8
2008 Nik-Zainal S, Holder SE, Cruwys M, Hall CM, Shaw-Smith C. Keipert syndrome: two further cases and review of the literature. Clinical Dysmorphology. 17: 169-75. PMID 18541962 DOI: 10.1097/MCD.0b013e3282f4afc3  0.8
2008 Al-Mudaffer M, Oley C, Price S, Hayes I, Stewart A, Hall CM, Reardon W. Clinical and radiological findings in Schinzel-Giedion syndrome. European Journal of Pediatrics. 167: 1399-407. PMID 18461363 DOI: 10.1007/s00431-008-0683-4  0.8
2008 Ang CW, Dawson R, Hall C, Farmer M. The diagnostic value of digital rectal examination in primary care for palpable rectal tumour. Colorectal Disease : the Official Journal of the Association of Coloproctology of Great Britain and Ireland. 10: 789-92. PMID 17868406 DOI: 10.1111/j.1463-1318.2007.01381.x  0.8
2008 Goodman SH, Broth MR, Hall CM, Stowe ZN. Treatment of postpartum depression in mothers: Secondary benefits to the infants Infant Mental Health Journal. 29: 492-513. DOI: 10.1002/imhj.20188  0.8
2008 Swanson G, Beckett C, Lovecchio S, Hall C. Cancer staging: Achieving compliance with Commission on Cancer standards Community Oncology. 5: 549-551.  0.8
2007 Rossi M, D'Armiento M, Parisi I, Ferrari P, Hall CM, Cervasio M, Rivasi F, Balli F, Vecchione R, Corso G, Andria G, Parenti G. Clinical phenotype of lathosterolosis. American Journal of Medical Genetics. Part A. 143: 2371-81. PMID 17853487 DOI: 10.1002/ajmg.a.31929  0.8
2007 Park SM, Hall CM, Gray R, Firth HV. Persistent upper airway obstruction is a diagnostic feature of spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type) with further evidence for dominant inheritance. American Journal of Medical Genetics. Part A. 143: 2024-8. PMID 17676604 DOI: 10.1002/ajmg.a.31857  0.8
2007 Dabir T, Sills AM, Hall CM, Bennett C, Wilson LC, Hennekam RC. Cranio-osteoarthropathy in sibs. Clinical Dysmorphology. 16: 197-201. PMID 17551338 DOI: 10.1097/MCD.0b013e32801470d8  0.8
2007 Zankl A, Jackson GC, Crettol LM, Taylor J, Elles R, Mortier GR, Spranger J, Zabel B, Unger S, Merrer ML, Cormier-Daire V, Hall CM, Wright MJ, Bonafe L, Superti-Furga A, et al. Preselection of cases through expert clinical and radiological review significantly increases mutation detection rate in multiple epiphyseal dysplasia. European Journal of Human Genetics : Ejhg. 15: 150-4. PMID 17133256 DOI: 10.1038/sj.ejhg.5201744  0.8
2007 Superti-Furga A, Unger S, Beighton P, Bonafé L, Braverman N, Briggs M, Cohn D, Cormier-Dairé V, Francomano C, Hall C, Horton W, Kaitila I, Krakow D, Lachman R, Lee B, et al. Nosology and classification of genetic skeletal disorders: 2006 Revision American Journal of Medical Genetics, Part A. 143: 1-18. PMID 17120245 DOI: 10.1002/ajmg.a.31483  0.8
2007 Bahar A, Whitby P, Holley S, Hoban PR, Elder JB, Deakin M, Hall C, Clayton RN, Williams GT, Farrell WE. Primary colorectal tumors fail to express the proapoptotic mediator PTAG and its reexpression augments drug-induced apoptosis. Genes, Chromosomes & Cancer. 46: 202-12. PMID 17117413 DOI: 10.1002/gcc.20401  0.8
2007 Hall C, Thomson P, Russell L. Teaching like an artist: The pedagogic identities and practices of artists in schools British Journal of Sociology of Education. 28: 605-619. DOI: 10.1080/01425690701505466  0.8
2007 Hall C, Thomson P. Creative partnerships? Cultural policy and inclusive arts practice in one primary school British Educational Research Journal. 33: 315-329. DOI: 10.1080/01411920701243586  0.8
2007 Hall C, Youens B. Re-forming the teaching work force: The case of the academic coach Educational Review. 59: 161-178. DOI: 10.1080/00131910701254932  0.8
2007 Young J, Hall C, Clarke T. Challenges to university autonomy in initial teacher education programmes: The cases of England, Manitoba and British Columbia Teaching and Teacher Education. 23: 81-93. DOI: 10.1016/j.tate.2006.04.008  0.8
2006 Sellick GS, Hoornaert KP, Mortier GR, King C, Dolling CL, Newbury-Ecob RA, Gargan M, Hall CM, Houlston RS, Smithson SF. A form of autosomal dominant spondyloepiphyseal dysplasia is caused by a glycine to alanine substitution in the COL2A1 gene. Clinical Dysmorphology. 15: 197-202. PMID 16957471 DOI: 10.1097/01.mcd.0000220616.55402.03  0.8
2006 Chitty LS, Tan AW, Nesbit DL, Hall CM, Rodeck CH. Sonographic diagnosis of SEDC and double heterozygote of SEDC and achondroplasia--a report of six pregnancies. Prenatal Diagnosis. 26: 861-5. PMID 16874841 DOI: 10.1002/pd.1525  0.8
2006 Thomas ER, Wakeling EL, Goodman FR, Dickinson JC, Hall CM, Brady AF. Mild case of Curry-Jones syndrome. Clinical Dysmorphology. 15: 115-7. PMID 16531740 DOI: 10.1097/01.mcd.0000194406.85052.de  0.8
2006 Deshpande C, Forrest M, Russell-Eggitt I, Hall CM, Mehta R, Paterson J. Visual impairment and prolonged survival in a girl with Marshall-Smith syndrome. Clinical Dysmorphology. 15: 111-3. PMID 16531739 DOI: 10.1097/01.mcd.0000194408.30794.2f  0.8
2006 Horsnell K, Ali M, Malik S, Wilson L, Hall C, Debeer P, Crow Y. Clinical phenotype associated with homozygosity for a HOXD13 7-residue polyalanine tract expansion European Journal of Medical Genetics. 49: 396-401. PMID 16497573 DOI: 10.1016/j.ejmg.2006.01.004  0.8
2006 Offiah AC, Moon L, Hall CM, Todd-Pokropek A. Diagnostic accuracy of fracture detection in suspected non-accidental injury: the effect of edge enhancement and digital display on observer performance. Clinical Radiology. 61: 163-73. PMID 16439222 DOI: 10.1016/j.crad.2005.09.004  0.8
2006 Hall CM. Narrative as vital methodology in clinical sociology Journal of Applied Social Science. 23: 53-67.  0.8
2005 Offiah AC, Grehan J, Hall CM, Todd-Pokropek A. Optimal exposure parameters for digital radiography of the infant skull: a pilot study. Clinical Radiology. 60: 1195-204. PMID 16223616 DOI: 10.1016/j.crad.2005.06.009  0.8
2005 Offiah AC, Woo P, Prieur AM, Hasson N, Hall CM. Camptodactyly-arthropathy-coxa vara-pericarditis syndrome versus juvenile idiopathic arthropathy. Ajr. American Journal of Roentgenology. 185: 522-9. PMID 16037531 DOI: 10.2214/ajr.185.2.01850522  0.8
2005 Venkat-Raman N, Sebire NJ, Murphy KW, Carvalho JS, Hall CM. Increased first-trimester fetal nuchal translucency thickness in association with chondroectodermal dysplasia (Ellis-Van Creveld syndrome). Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 25: 412-4. PMID 15717287 DOI: 10.1002/uog.1849  0.8
2005 Rossi M, De Brasi D, Hall CM, Battagliese A, Melis D, Sebastio G, Andria G. A new familial case of spondylo-epi-metaphyseal dysplasia with multiple dislocations Hall type (leptodactylic form). Clinical Dysmorphology. 14: 13-8. PMID 15602087 DOI: 10.1097/00019605-200501000-00003  0.8
2005 Hall C. Experiences with a Disease Management Program | Erfahrungen mit einem Disease-Management-Programm Gesundheitsokonomie Und Qualitatsmanagement. 10: S23-S25. DOI: 10.1055/s-2005-858276  0.8
2004 O'Connell S, Suri M, Duff D, Kelleher J, Hall CM, Reardon W. Congenital cardiac disease as a core feature of cranio-osteoarthropathy. Clinical Dysmorphology. 13: 213-9. PMID 15365456 DOI: 10.1097/00019605-200410000-00003  0.8
2004 Shears DJ, Offiah A, Rutland P, Sirimanna T, Bitner-Glindzicz M, Hall C. Kantaputra mesomelic dysplasia: A second reported family American Journal of Medical Genetics. 128: 6-11. PMID 15211647  0.8
2004 Holder-Espinasse M, Fayoux P, Morillon S, Fourier C, Dieux-Coeslier A, Manouvrier-Hanu S, Le Merrer M, Hall CM. Spondyloepimetaphyseal dysplasia (Hall type) with laryngeal stenosis: a new diagnostic feature? Clinical Dysmorphology. 13: 133-5. PMID 15194947 DOI: 10.1097/01.mcd.0000130236.02981.c5  0.8
2004 Johnson K, Chapman S, Hall CM. Skeletal injuries associated with sexual abuse. Pediatric Radiology. 34: 620-3. PMID 15156299 DOI: 10.1007/s00247-004-1216-6  0.8
2004 Hall C, Nester CJ. Sagittal plane compensations for artificially induced limitation of the first metatarsophalangeal joint: A preliminary study Journal of the American Podiatric Medical Association. 94: 269-274. PMID 15153589  0.8
2004 Wakeling EL, Cruwys M, Suri M, Brady AF, Aylett SE, Hall C. Central osteoclerosis with trichothiodystrophy Pediatric Radiology. 34: 541-546. PMID 15148554  0.8
2004 Young ID, Barrow M, Hall CM. Microcephalic osteodysplastic primordial short stature type II with café-au-lait spots and moyamoya disease: another patient. American Journal of Medical Genetics. Part A. 127: 218-20. PMID 15108216 DOI: 10.1002/ajmg.a.20647  0.8
2004 Wenaden AE, McHugh K, Hill RA, Hall CM. Pseudarthrosis presenting as a late complication of meningococcal septicaemia and disseminated intravascular coagulation. Skeletal Radiology. 33: 287-90. PMID 14997350 DOI: 10.1007/s00256-004-0747-0  0.8
2004 Hall CM, Elçioglu NH. Metatropic dysplasia lethal variants. Pediatric Radiology. 34: 66-74. PMID 14566438 DOI: 10.1007/s00247-003-1063-x  0.8
2004 Broth MR, Goodman SH, Hall C, Raynor LC. Depressed and well mothers' emotion interpretation accuracy and the quality of mother-infant interaction Infancy. 6: 37-55.  0.8
2003 Offiah AC, Hall CM. Evaluation of the Commission of the European Communities quality criteria for the paediatric lateral spine. The British Journal of Radiology. 76: 885-90. PMID 14711776 DOI: 10.1259/bjr/57437508  0.8
2003 Offiah AC, Mansour S, Jeffrey I, Nash R, Whittock N, Pyper R, Bewley S, Clayton PT, Hall CM. Greenberg dysplasia (HEM) and lethal X linked dominant Conradi-Hünermann chondrodysplasia punctata (CDPX2): presentation of two cases with overlapping phenotype. Journal of Medical Genetics. 40: e129. PMID 14684697  0.8
2003 Oosterwijk JC, Mansour S, van Noort G, Waterham HR, Hall CM, Hennekam RC. Congenital abnormalities reported in Pelger-Huët homozygosity as compared to Greenberg/HEM dysplasia: highly variable expression of allelic phenotypes. Journal of Medical Genetics. 40: 937-41. PMID 14684694  0.8
2003 Offiah AC, Hall CM. Observational study of skeletal surveys in suspected non-accidental injury. Clinical Radiology. 58: 702-5. PMID 12943642 DOI: 10.1016/S0009-9260(03)00226-5  0.8
2003 Sand O, Gingras M, Beck N, Hall C, Trun N. Phenotypic characterization of overexpression or deletion of the Escherichia coli crcA, cspE and crcB genes. Microbiology (Reading, England). 149: 2107-17. PMID 12904550  0.8
2003 Morgan NV, Bacchelli C, Gissen P, Morton J, Ferrero GB, Silengo M, Labrune P, Casteels I, Hall C, Cox P, Kelly DA, Trembath RC, Scambler PJ, Maher ER, Goodman FR, et al. A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13 Journal of Medical Genetics. 40: 431-435. PMID 12807964  0.8
2003 Hosalkar HS, Jones DH, Offiah A, Hall C. Linear sebaceous naevus syndrome and resistant rickets Journal of Bone and Joint Surgery - Series B. 85: 578-583. PMID 12793567 DOI: 10.1302/0301-620X.85B4.13483  0.8
2003 Offiah AC, Cornette L, Hall CM. Paternal uniparental disomy 14: introducing the "coat-hanger" sign. Pediatric Radiology. 33: 509-12. PMID 12712270 DOI: 10.1007/s00247-003-0931-8  0.8
2003 Offiah AC, Hall CM. Radiological diagnosis of the constitutional disorders of bone. As easy as A, B, C? Pediatric Radiology. 33: 153-61. PMID 12612812 DOI: 10.1007/s00247-002-0855-8  0.8
2003 Reardon W, Hall CM. Broad thumbs and halluces with deafness: a patient with Keipert syndrome. American Journal of Medical Genetics. Part A. 118: 86-9. PMID 12605449 DOI: 10.1002/ajmg.a.10063  0.8
2003 Offiah AC, Hall CM. Imaging of non-accidental injury Current Paediatrics. 13: 455-459. DOI: 10.1016/S0957-5839(03)00082-4  0.8
2002 Wilson LC, Hall CM. Albright's hereditary osteodystrophy and pseudohypoparathyroidism. Seminars in Musculoskeletal Radiology. 6: 273-83. PMID 12541184 DOI: 10.1055/s-2002-36726  0.8
2002 Nuwaysir EF, Huang W, Albert TJ, Singh J, Nuwaysir K, Pitas A, Richmond T, Gorski T, Berg JP, Ballin J, McCormick M, Norton J, Pollock T, Sumwalt T, Butcher L, ... ... Hall C, et al. Gene expression analysis using oligonucleotide arrays produced by maskless photolithography. Genome Research. 12: 1749-55. PMID 12421762 DOI: 10.1101/gr.362402  0.8
2002 Aldred MA, Aftimos S, Hall C, Waters KS, Thakker RV, Trembath RC, Brueton L. Constitutional deletion of chromosome 20q in two patients affected with albright hereditary osteodystrophy American Journal of Medical Genetics. 113: 167-172. PMID 12407707 DOI: 10.1002/ajmg.10751  0.8
2002 Suri M, Garrett C, Winter RM, Hall CM, Griffiths M. Dysplastic cortical hyperostosis (Kozlowski-Tsuruta syndrome): report of a second case. Clinical Dysmorphology. 11: 267-70. PMID 12401992  0.8
2002 Hall CM. International nosology and classification of constitutional disorders of bone (2001). American Journal of Medical Genetics. 113: 65-77. PMID 12400068 DOI: 10.1002/ajmg.10828  0.8
2002 Elçioglu NH, Hall CM. Diagnostic dilemmas in the short rib-polydactyly syndrome group. American Journal of Medical Genetics. 111: 392-400. PMID 12210298 DOI: 10.1002/ajmg.10562  0.8
2002 Offiah AC, Mansour S, McDowall S, Tolmie J, Sim P, Hall CM. Surviving campomelic dysplasia has the radiological features of the previously reported ischio-pubic-patella syndrome. Journal of Medical Genetics. 39: e50. PMID 12205120  0.8
2002 Hall CM, Elcioglu NH, MacDermot KD, Offiah AC, Winter RM. Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance. Journal of Medical Genetics. 39: 666-70. PMID 12205110  0.8
2002 Elçioglu NH, Vellodi A, Hall CM. Dysosteosclerosis: a report of three new cases and evolution of the radiological findings. Journal of Medical Genetics. 39: 603-7. PMID 12161605  0.8
2002 Mansour S, Offiah AC, McDowall S, Sim P, Tolmie J, Hall C. The phenotype of survivors of campomelic dysplasia Journal of Medical Genetics. 39: 597-602. PMID 12161603  0.8
2002 Aviv RI, Rodger E, Hall CM. Craniosynostosis. Clinical Radiology. 57: 93-102. PMID 11977940 DOI: 10.1053/crad.2001.0836  0.8
2002 Goodship JA, O'Sullivan J, Chinnery PF, Ryan AK, Ziakas N, Hall CM, Clarke M. Dilated cardiomyopathy, sudden cardiac death, hypoplastic discs, and retinal detachment: a new autosomal dominant syndrome. Journal of Medical Genetics. 39: 221-3. PMID 11897830  0.8
2002 Bates AW, Hall CM, Morgan H, Rosser EM, Scheimberg I. Lethal acrofacial dysostosis, pre- and post-axial defects of the hands, and bilateral renal agenesis. Clinical Dysmorphology. 11: 63-6. PMID 11822708  0.8
2002 Brennan P, Hall C. Osteocraniostenosis in a fetus with a 46,XX/46,XY karyotype Clinical Dysmorphology. 11: 57-61. PMID 11822707  0.8
2002 Comolli JC, Carl AJ, Hall C, Donohue T. Transcriptional activation of the Rhodobacter sphaeroides cytochrome c2 gene P2 promoter by the response regulator PrrA Journal of Bacteriology. 184: 390-399. PMID 11751815 DOI: 10.1128/JB.184.2.390-399.2002  0.8
2001 Offiah AC, Lees M, Winter RM, Hall CM. Sponastrime dysplasia: presentation in infancy. Journal of Medical Genetics. 38: 889-93. PMID 11768397  0.8
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