Evidence suggesting the inheritance mode of the humanP gene in skin complexion is not strictly recessive-Reference-Cited by-同舟云学术

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Evidence suggesting the inheritance mode of the humanP gene in skin complexion is not strictly recessive

Published:2008 Issue:11 Volume:146A Page:1493-1496
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Chiang Pei-Wen,Spector Elaine,Tsai Anne Chun-Hui

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome

2. Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of theP gene

3. Diagnosis of Angelman syndrome in infants

4. The Mouse Pink-Eyed Dilution Gene: Association with Human Prader-Willi and Angelman Syndromes

Cited by 11 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. Nystagmus and Foveal Hypoplasia in a Carrier of Oculocutaneous Albinism;Ophthalmic Surgery, Lasers and Imaging Retina;2024-06

2. A small gene sequencing panel realises a high diagnostic rate in patients with congenital nystagmus following basic phenotyping;Scientific Reports;2019-09-13

3. Comprehensive Review of the Genetics of Albinism;Journal of Visual Impairment & Blindness;2018-11

4. Identification of a functionally significant tri-allelic genotype in the Tyrosinase gene (TYR) causing hypomorphic oculocutaneous albinism (OCA1B);Scientific Reports;2017-06-30

5. Angelman syndrome and severe infections in a patient with de novo 15q11.2–q13.1 deletion and maternally inherited 2q21.3 microdeletion;Gene;2013-01

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