Patricia L. Crotwell, Ph.D. - Publications

University of South Dakota, Vermillion, SD, United States 

2/19 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
2007 Crotwell PL, Mabee PM. Gene expression patterns underlying proximal-distal skeletal segmentation in late-stage zebrafish, Danio rerio. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 236: 3111-28. PMID 17948314 DOI: 10.1002/Dvdy.21352  0.24
2004 Crotwell PL, Sommervold AR, Mabee PM. Expression of bmp2a and bmp2b in late-stage zebrafish median fin development. Gene Expression Patterns : Gep. 5: 291-6. PMID 15567728 DOI: 10.1016/J.Modgep.2004.07.001  0.24
Low-probability matches
2001 Crotwell PL, Clark TG, Mabee PM. Gdf5 is expressed in the developing skeleton of median fins of late-stage zebrafish, Danio rerio. Development Genes and Evolution. 211: 555-8. PMID 11862461 DOI: 10.1007/S00427-001-0186-Z  0.24
2016 Madeo M, Stewart M, Sun Y, Sahir N, Wiethoff S, Chandrasekar I, Yarrow A, Rosenfeld JA, Yang Y, Cordeiro D, McCormick EM, Muraresku CC, Jepperson TN, McBeth LJ, Seidahmed MZ, ... ... Crotwell PL, et al. Loss-of-Function Mutations in FRRS1L Lead to an Epileptic-Dyskinetic Encephalopathy. American Journal of Human Genetics. PMID 27236917 DOI: 10.1016/J.Ajhg.2016.04.008  0.24
2015 Flanagan JD, Reuter S, Crotwell PL, Myers A, De Berg K. A Hutterite condition that mimics Bowen-Conradi syndrome. South Dakota Medicine : the Journal of the South Dakota State Medical Association. 68: 101-3. PMID 25906497  0.24
2014 Somsen D, Davis-Keppen L, Crotwell P, Flanagan J, Munson P, Stein Q. Congenital nasal pyriform aperture stenosis and ocular albinism co-occurring in a sibship with a maternally-inherited 97 kb Xp22.2 microdeletion. American Journal of Medical Genetics. Part A. 164: 1268-71. PMID 24478262 DOI: 10.1002/Ajmg.A.36415  0.24
2013 Kruer MC, Jepperson TN, Weimer JM, Mroch A, Davis-Keppen L, Crotwell P, Parboosingh J. Mutations in VLDLR associated with ataxia with secondary vitamin E deficiency. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1904-5. PMID 23813796 DOI: 10.1002/Mds.25573  0.24
2002 Mabee PM, Crotwell PL, Bird NC, Burke AC. Evolution of median fin modules in the axial skeleton of fishes. The Journal of Experimental Zoology. 294: 77-90. PMID 12210109 DOI: 10.1002/Jez.10076  0.24
2017 Reed JA, Crotwell PL, Stein Q, Mroch A, Davis-Keppen L, Khan A. Case Report of Infant With Features of Beckwith-Wiedemann Syndrome Diagnosed With Genome-wide Uniparental Disomy. South Dakota Medicine : the Journal of the South Dakota State Medical Association. 70: 505-509. PMID 29088522  0.01
2016 Masuho I, Fang M, Geng C, Zhang J, Jiang H, Özgul RK, Yılmaz DY, Yalnızoğlu D, Yüksel D, Yarrow A, Myers A, Burn SC, Crotwell PL, Padilla-Lopez S, Dursun A, et al. Homozygous GNAL mutation associated with familial childhood-onset generalized dystonia. Neurology. Genetics. 2: e78. PMID 27222887 DOI: 10.1212/Nxg.0000000000000078  0.01
2015 Salih MA, Seidahmed MZ, El Khashab HY, Hamad MH, Bosley TM, Burn S, Myers A, Landsverk ML, Crotwell PL, Bilguvar K, Mane S, Kruer MC. Mutation in GM2A Leads to a Progressive Chorea-dementia Syndrome. Tremor and Other Hyperkinetic Movements (New York, N.Y.). 5: 306. PMID 26203402 DOI: 10.7916/D8D21WQ0  0.01
2015 Torbert N, Reuter S, Myers A, De Berg K, Crotwell PL, Flanagan JD. Bowen-Conradi Syndrome: a trisomy 18-like autosomal recessive disorder common in Hutterites. South Dakota Medicine : the Journal of the South Dakota State Medical Association. 68: 65-7, 69. PMID 25799636  0.01
2013 Blake J, Hoyme HE, Crotwell PL. A brief history of autism, the autism/vaccine hypothesis and a review of the genetic basis of autism spectrum disorders. South Dakota Medicine : the Journal of the South Dakota State Medical Association. 58-65. PMID 23444593  0.01
2012 Flanagan JD, Stein QP, Mroch AR, Deberg KL, Crotwell PL, Keppen LD. Bowen-Conradi: a common Hutterite condition that mimics trisomy 18. South Dakota Medicine : the Journal of the South Dakota State Medical Association. 65: 221-3, 225. PMID 22856010  0.01
2012 Crotwell PL, Hoyme HE. Advances in whole-genome genetic testing: from chromosomes to microarrays. Current Problems in Pediatric and Adolescent Health Care. 42: 47-73. PMID 22325474 DOI: 10.1016/j.cppeds.2011.10.004  0.01
2012 Crotwell PL, Eugene Hoyme H. Core concepts: Chromosome aneuploidies Neoreviews. 13: e30-e39. DOI: 10.1542/neo.13-1-e30  0.01
2008 Stein QP, Boyle JG, Crotwell PL, Flanagan JD, Johnson KJ, Davis-Keppen L, Van Eerden P, Woltanski AR, Watson WJ. Prenatally diagnosed trisomy 20 mosaicism associated with arachnoid cyst of basal cistern. Prenatal Diagnosis. 28: 1169-70. PMID 19003786 DOI: 10.1002/Pd.2147  0.01
2008 Mello AL, Crotwell PL, Flanagan JD, Woltanski AR, Keppen LD, Van Eerden P, Boyle JG, Stein Q. Clinical course of a 20-month-old child diagnosed prenatally with mosaic ring chromosome 18 and monosomy 18. South Dakota Medicine : the Journal of the South Dakota State Medical Association. 61: 327-9, 331. PMID 18935916  0.01
2001 CROTWELL P. THE WONDERFUL WORLD OF CICHLIDS Bioscience. 51: 410. DOI: 10.1641/0006-3568(2001)051[0410:Twwoc]2.0.Co;2  0.01
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