Found: 18
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Segregation analysis of autosomal dominant polycystic kidney disease.
- Published in:
- Genetic Epidemiology, 1993, v. 10, n. 3, p. 189, doi. 10.1002/gepi.1370100305
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- Publication type:
- Article
Genetic features of hearing loss associated with ear anomalies: PDS and EYA1 mutation analysis.
- Published in:
- Journal of Human Genetics, 2001, v. 46, n. 9, p. 518, doi. 10.1007/s100380170033
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- Publication type:
- Article
Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss: KCNQ4 is a gene responsible in Japanese.
- Published in:
- Journal of Human Genetics, 2001, v. 46, n. 7, p. 355, doi. 10.1007/s100380170053
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- Publication type:
- Article
Isepamicin sulfate-induced sensorineural hearing loss in patients with the 1555 A-->G mitochondrial mutation.
- Published in:
- 1998
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- Publication type:
- journal article
Familial heterogeneity of colon cancer risk.
- Published in:
- 1986
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- Publication type:
- journal article
Genetics and smoking-associated cancers. A study of 485 families.
- Published in:
- 1986
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- Publication type:
- journal article
Hereditary nonpolyposis colorectal cancer (Lynch syndromes I and II). II. Biomarker studies.
- Published in:
- 1985
- By:
- Publication type:
- journal article
Hereditary ovarian carcinoma. Biomarker studies.
- Published in:
- 1985
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- Publication type:
- journal article
Natural history of hereditary cancer of the breast and colon.
- Published in:
- 1982
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- Publication type:
- journal article
THE GENETICS OF AN EXPANDED SECRETOR SYSTEM.
- Published in:
- International Journal of Immunogenetics, 1979, v. 6, n. 2, p. 75, doi. 10.1111/j.1744-313X.1979.tb00332.x
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- Publication type:
- Article
Spelling errors in adults with a form of familial dyslexia.
- Published in:
- 1986
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- Publication type:
- journal article
The Search for Branchiootorenal Syndrome on Chromosomes 1 and 8.
- Published in:
- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 288, doi. 10.1111/j.1749-6632.1991.tb19607.x
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- Publication type:
- Article
Genetic Studies of Usher Syndrome.
- Published in:
- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 167, doi. 10.1111/j.1749-6632.1991.tb19585.x
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- Publication type:
- Article
Report on Attempts to Localize Usher Syndrome Type 1 by Linkage Analysis to Selected Candidate Regions.
- Published in:
- Annals of the New York Academy of Sciences, 1991, v. 630, n. 1, p. 298, doi. 10.1111/j.1749-6632.1991.tb19612.x
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- Publication type:
- Article
Racial differences in the frequency of Q and C chromosomal heteromorphisms.
- Published in:
- Nature, 1977, v. 268, n. 5621, p. 631, doi. 10.1038/268631a0
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- Publication type:
- Article
Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation.
- Published in:
- Clinical Genetics, 2010, v. 77, n. 6, p. 563, doi. 10.1111/j.1399-0004.2009.01344.x
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- Publication type:
- Article
Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Biochemical and cytogenetic techniques for the study of communication disorders.
- Published in:
- 1981
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- Publication type:
- journal article