Homozygosity in piebald trait.-Reference-Cited by-同舟云学术

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Homozygosity in piebald trait.

Published:1987-09-01 Issue:9 Volume:24 Page:568-571
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Hulten M A,Honeyman M M,Mayne A J,Tarlow M J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. Mendel's principles of heredity;Bateson, W.

2. Dominance and homozygosity in man;Pauli, R.M.;Am J Med Genet,1983

3. Dominance and homozygosity in man;Hirschhorn, K.;Am J Med Genet,1984

4. Mendelian inheritance in man. Catalog of autosomal dominant, autosomal recessive, and X-linked phenotypes;McKusick, V.A.,1983

5. Partial albinism;GF, Comings D.E.Odland;JAMA,1966

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Piebaldism with café‐au‐lait macules resulting from a novel mutation of KIT gene in a three‐generation Chinese family;Skin Research and Technology;2023-05-25

2. Congenital Sensorineural Hearing Loss and Inborn Pigmentary Disorders: First Report of Multilocus Syndrome in Piebaldism;Medicina;2019-07-07

3. In-frame Val 216 -Ser 217 deletion of KIT in mild piebaldism causes aberrant secretion and SCF response;Journal of Dermatological Science;2018-07

4. A novel mutation of KIT gene results in piebaldism in a Chinese family;Journal of the European Academy of Dermatology and Venereology;2014-09-08

5. Homozygosity for piebaldism with a proven KIT mutation resulting in depigmentation of the skin and hair, deafness, developmental delay and autism spectrum disorder;Clinical Dysmorphology;2013-04

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