| Year |
Citation |
Score |
| 1998 |
Tolarová MM, Cervenka J. Classification and birth prevalence of orofacial clefts. American Journal of Medical Genetics. 75: 126-37. PMID 9450872 DOI: 10.1002/(Sici)1096-8628(19980113)75:2<126::Aid-Ajmg2>3.0.Co;2-R |
0.339 |
|
| 1996 |
Thomas JT, Lin K, Nandedkar M, Camargo M, Cervenka J, Luyten FP. A human chondrodysplasia due to a mutation in a TGF-beta superfamily member. Nature Genetics. 12: 315-7. PMID 8589725 DOI: 10.1038/ng0396-315 |
0.402 |
|
| 1992 |
Lobo S, Cervenka J, London A, Pierpont ME. Interstitial deletion of 10q: clinical features and literature review. American Journal of Medical Genetics. 43: 701-3. PMID 1621761 DOI: 10.1002/Ajmg.1320430410 |
0.422 |
|
| 1990 |
Kurvink K, Cervenka J. Acrocentric prophasing in bromodeoxyuridine-incorporated chromosomes. Cancer Genetics and Cytogenetics. 50: 265-71. PMID 2265405 |
0.325 |
|
| 1989 |
Langer LO, Cervenka J, Camargo M. A severe autosomal recessive acromesomelic dysplasia, the Hunter-Thompson type, and comparison with the Grebe type. Human Genetics. 81: 323-8. PMID 2703235 DOI: 10.1007/Bf00283684 |
0.499 |
|
| 1988 |
Witkop CJ, Keenan KM, Cervenka J, Jaspers MT. Taurodontism: an anomaly of teeth reflecting disruptive developmental homeostasis. American Journal of Medical Genetics. Supplement. 4: 85-97. PMID 3144989 DOI: 10.1002/Ajmg.1320310513 |
0.351 |
|
| 1987 |
Cervenka J, Camargo M. Premature chromosome condensation induced by electrofusion. Cytogenetics and Cell Genetics. 45: 169-73. PMID 3691182 |
0.535 |
|
| 1986 |
Krawczun MS, Camargo M, Cervenka J. Patterns of BrdU incorporation in homogeneously staining regions and double minutes. Cancer Genetics and Cytogenetics. 21: 257-65. PMID 2418948 DOI: 10.1016/0165-4608(86)90006-3 |
0.537 |
|
| 1985 |
Schaumann B, Satish J, Johnson SB, Moore K, Cervenka J. Effects of carbamazepine on human chromosomes. Epilepsia. 26: 346-52. PMID 4006894 DOI: 10.1111/J.1528-1157.1985.Tb05661.X |
0.327 |
|
| 1984 |
Camargo M, Cervenka J. DNA replication and inactivation patterns in structural abnormality of sex chromosomes. I.X-A translocations, rings, fragments, isochromosomes, and pseudo-isodicentrics. Human Genetics. 67: 37-47. PMID 6745924 DOI: 10.1007/Bf00270556 |
0.592 |
|
| 1984 |
Krawczun M, Melink G, Cervenka J. Ring chromosome 14 and immunoglobulin locus. American Journal of Medical Genetics. 17: 465-9. PMID 6702898 DOI: 10.1002/Ajmg.1320170209 |
0.41 |
|
| 1984 |
Nagel T, Camargo M, Tagatz G, Okagaki T, Cervenka J, Cahill L, Wachtel SS, King R, Twiggs LB. Gonadal tumors in patients with gonadal dysgenesis and sex chromosomal rings and fragments. American Journal of Obstetrics and Gynecology. 150: 76-82. PMID 6476029 |
0.512 |
|
| 1983 |
Cervenka J, Hirsch BA. Cytogenetic differentiation of Fanconi anemia, "idiopathic" aplastic anemia, and Fanconi anemia heterozygotes. American Journal of Medical Genetics. 15: 211-23. PMID 6410915 DOI: 10.1002/Ajmg.1320150205 |
0.376 |
|
| 1982 |
Wiencke JK, Cervenka J, Kennedy BJ, Prlina J, Gorlin R. Sister-chromatid exchange induction by cis-platinum/adriamycin cancer chemotherapy. Mutation Research. 104: 131-6. PMID 7200570 DOI: 10.1016/0165-7992(82)90133-6 |
0.397 |
|
| 1982 |
Camargo M, Cervenka J. Patterns of DNA replication of human chromosomes. II. Replication map and replication model. American Journal of Human Genetics. 34: 757-80. PMID 7124731 |
0.548 |
|
| 1982 |
Johnson MP, Ramsay N, Cervenka J, Wang N. Retinoblastoma and its association with a deletion in chromosome #13: a survey using high-resolution chromosome techniques. Cancer Genetics and Cytogenetics. 6: 29-37. PMID 7104985 DOI: 10.1016/0165-4608(82)90018-8 |
0.453 |
|
| 1982 |
Gorlin RJ, Cervenka J, Bloom BA, Langer LO. No chromosome deletion found on prometaphase banding in two cases of Langer-Giedion syndrome. American Journal of Medical Genetics. 13: 345-7. PMID 6983832 DOI: 10.1002/ajmg.1320130322 |
0.55 |
|
| 1981 |
Camargo M, Johnson MP, Cervenka J. Delineation of 13q-deletion by replication banding in retinoblastoma. Cytogenetics and Cell Genetics. 31: 77-83. PMID 7307584 DOI: 10.1159/000131628 |
0.581 |
|
| 1981 |
Tsuchiya H, Kobayashi S, Cervenka J, Mori H, Oguro A. Analysis of the dentition and orofacial skeleton in Seckel's bird-headed dwarfism. Journal of Maxillofacial Surgery. 9: 170-5. PMID 6944418 DOI: 10.1016/S0301-0503(81)80038-0 |
0.352 |
|
| 1980 |
Camargo M, Cervenka J. Pattern of chromosomal replication in synchronized lymphocytes. I. Evaluation and application of methotrexate block. Human Genetics. 54: 47-53. PMID 6993339 DOI: 10.1007/Bf00279048 |
0.585 |
|
| 1979 |
Cervenka J, Witkop CJ, Okoro AN, King RA. Chromosome breaks and sister chromatid exchanges in albinos in Nigeria. Clinical Genetics. 15: 17-21. PMID 759053 DOI: 10.1111/J.1399-0004.1979.Tb02024.X |
0.405 |
|
| 1979 |
Wiencke JK, Cervenka J, Paulus H. Mutagenic activity of anticancer agent cis-dichlorodiammine platinum-II. Mutation Research. 68: 69-77. PMID 492199 DOI: 10.1016/0165-1218(79)90079-X |
0.307 |
|
| 1979 |
Cervenka J, Tsuchiya H, Ishiki T, Suzuki M, Mori H. Seckel's dwarfism: analysis of chromosome breakage and sister chromatid exchanges. American Journal of Diseases of Children (1960). 133: 555-6. PMID 433882 DOI: 10.1001/Archpedi.1979.02130050099023 |
0.39 |
|
| 1978 |
Larsen RE, Dias E, Cervenka J. Centric fusion of autosomal chromosomes in a bitch and offspring. American Journal of Veterinary Research. 39: 861-4. PMID 727590 |
0.325 |
|
| 1978 |
Kurvink K, Bloomfield CD, Cervenka J. Sister chromatid exchange in patients with viral disease. Experimental Cell Research. 113: 450-3. PMID 233771 DOI: 10.1016/0014-4827(78)90389-0 |
0.306 |
|
| 1977 |
Cervenka J, Anderson RS, Nesbit ME, Krivit W. Familial leukemia and inherited chromosomal aberration. International Journal of Cancer. Journal International Du Cancer. 19: 783-8. PMID 873642 DOI: 10.1002/Ijc.2910190607 |
0.427 |
|
| 1977 |
Burgdorf W, Kurvink K, Cervenka J. Elevated sister chromatid exchange rate in lymphocytes of subjects treated with arsenic. Human Genetics. 36: 69-72. PMID 870411 DOI: 10.1007/Bf00390438 |
0.332 |
|
| 1977 |
Cervenka J, Hansen CA, Franciosi RA, Gorlin RJ. Trisomy 22 with 'cat eye' anomaly. Journal of Medical Genetics. 14: 288-90. PMID 336892 |
0.522 |
|
| 1977 |
Gorlin RJ, Cervenka J, Cohen MM. "Newer" facial clefting syndromes. Birth Defects Original Article Series. 13: 1-9. PMID 329913 |
0.457 |
|
| 1977 |
Vance JC, Cervenka J, Ullman S, Kersey JH, Sabad A, Green N. Immunological and chromosomal studies in a patient with Sézary syndrome. Archives of Dermatology. 113: 1417-23. PMID 143911 DOI: 10.1001/Archderm.1977.01640100095019 |
0.412 |
|
| 1977 |
Cervenka J, Gorlin RJ, Djavadi GR. Down syndrome due to partial trisomy 21q. Clinical Genetics. 11: 119-21. PMID 138496 DOI: 10.1111/J.1399-0004.1977.Tb01288.X |
0.608 |
|
| 1976 |
Bushkell LL, Kersey JH, Cervenka J. Chromosomal breaks in T and B lymphocytes in Fanconi's anemia. Clinical Genetics. 9: 583-7. PMID 1084238 DOI: 10.1111/J.1399-0004.1976.Tb01616.X |
0.338 |
|
| 1976 |
Cervenka J, Djavadi GR, Gorlin RJ. Partial trisomy 4q syndrome: case report and review. Human Genetics. 34: 1-7. PMID 964997 DOI: 10.1007/Bf00284426 |
0.597 |
|
| 1976 |
Cervenka J. Chromosomal considerations--application of modern cytogenetics. International Dental Journal. 26: 391-7. PMID 62717 |
0.307 |
|
| 1975 |
Gorlin RJ, Cervenka J. Alopecia totalis, nail dysplasia and amelogenesis imperfecta. Birth Defects Original Article Series. 11: 23-4. PMID 1218220 |
0.509 |
|
| 1975 |
Gorlin RJ, Cervenka J, Moller K, Horrobin M, Witkop CJ. Malformation syndromes. A selected miscellany. Birth Defects Original Article Series. 11: 39-50. PMID 819054 |
0.433 |
|
| 1974 |
Cervenka J, Thorn HL. Chromosomes and spray adhesivess. The New England Journal of Medicine. 290: 543-5. PMID 4811100 DOI: 10.1056/Nejm197403072901005 |
0.418 |
|
| 1974 |
Gorlin RJ, Cervenka J. Syndromes of facial clefting. Scandinavian Journal of Plastic and Reconstructive Surgery. 8: 13-25. PMID 4615366 DOI: 10.3109/02844317409084366 |
0.511 |
|
| 1974 |
Schaumann B, Cervenka J, Gorlin RJ. Dermatoglyphics in trisomy 8 mosaicism. Human Genetics. 24: 201-205. PMID 4442867 DOI: 10.1007/Bf00283585 |
0.394 |
|
| 1974 |
Cervenka J, Ballin R. Tissue Culture and Chromosomal Analysis of Dental Pulp Cells Journal of Dental Research. 53: 768-768. DOI: 10.1177/00220345740530034801 |
0.35 |
|
| 1973 |
Cervenka J, Thorn HL, Gorlin RJ. Structural basis of banding pattern of human chromosomes. Cytogenetics and Cell Genetics. 12: 81-6. PMID 4123125 DOI: 10.1159/000130442 |
0.532 |
|
| 1971 |
Cervenka J, Jacobson DE, Gorlin RJ. Determination of "Y body" from hair-root sheaths of males. The New England Journal of Medicine. 284: 856-7. PMID 5549820 |
0.351 |
|
| 1971 |
Duffy JC, Cervenka J. Search for XYY syndrome in psychiatrically disturbed children and adolescent juvenile delinquents. A preliminary report. Child Psychiatry and Human Development. 2: 50-3. PMID 5163298 DOI: 10.1007/Bf01442059 |
0.39 |
|
| 1971 |
Gorlin RJ, Cervenka J, Pruzansky S. Facial clefting and its syndromes. Birth Defects Original Article Series. 7: 3-49. PMID 4950925 |
0.457 |
|
| 1971 |
Cervenka J, Gorlin RJ, Bendel RP. Prenatal sex determination. Detection of "Y body". Obstetrics and Gynecology. 37: 912-5. PMID 4378218 |
0.372 |
|
| 1971 |
Cervenka J. Identification of human G-group and Y chromosomes. Demonstration of constitutive heterochromatin by modified DNA-RNA hybridization technique. Clinical Genetics. 2: 375-8. PMID 4264351 DOI: 10.1111/J.1399-0004.1971.Tb00299.X |
0.449 |
|
| 1971 |
Cervenka J, Jacobson DE, Gorlin RJ. Fluorescing structures of human metaphase chromosomes. Detection of "Y body". American Journal of Human Genetics. 23: 317-24. PMID 4103775 |
0.457 |
|
| 1970 |
Gorlin RJ, Cervenka J, Anderson RC, Sauk JJ, Bevis WD. Robin's syndrome. A probably X-linked recessive subvariety exhibiting persistence of left superior vena cava and atrial septal defect. American Journal of Diseases of Children (1960). 119: 176-8. PMID 5410571 DOI: 10.1001/Archpedi.1970.02100050178020 |
0.529 |
|
| 1970 |
Cervenka J, Gorlin RJ, Figalova P, Farkasova J. Craniocarpotarsal dysplasia or whistling face syndrome. Archives of Otolaryngology (Chicago, Ill. : 1960). 91: 183-7. PMID 5410086 DOI: 10.1001/Archotol.1970.00770040253016 |
0.529 |
|
| 1969 |
Cervenka J, Figalová P, Gorlin RJ. Cranio-carpo-tarsal dysplasia or the whistling face syndrome. II. Oral intercommissural distance in children. American Journal of Diseases of Children (1960). 117: 434-5. PMID 5773411 DOI: 10.1001/Archpedi.1969.02100030436008 |
0.47 |
|
| 1968 |
Gorlin RJ, Sedano HO, Vickers RA, Cervenka J. Multiple mucosal neuromas, pheochromocytoma and medullary carcinoma of the thyroid--a syndrome. Cancer. 22: 293-9 passim. PMID 5660196 DOI: 10.1002/1097-0142(196808)22:2<293::Aid-Cncr2820220206>3.0.Co;2-R |
0.484 |
|
| 1968 |
Gorlin RJ, Sedano HO, Cervenka J. Popliteal pterygium syndrome . A syndrome comprising cleft lip-palate, popliteal and intercrural pterygia, digital and genital anomalies. Pediatrics. 41: 503-9. PMID 4384166 |
0.466 |
|
| 1967 |
Cervenka J, Gorlin RJ, Anderson VE. The syndrome of pits of the lower lip and cleft lip and/or palate. Genetic considerations. American Journal of Human Genetics. 19: 416-32. PMID 6026934 |
0.435 |
|
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