Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): Further evidence of localization at Xp11-Reference-Cited by-同舟云学术

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Incontinentia pigmenti achromians (hypomelanosis of ITO, MIM 146150): Further evidence of localization at Xp11

Published:1993-06-15 Issue:5 Volume:46 Page:529-533
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Koiffmann Célia P.,de Souza Deise H.,Diament Aron,Ventura Heloisa B.,Alves Rosana S.,Kihara Sonia,Wajntal Anita

Publisher

Wiley

Subject

Genetics (clinical)

Reference24 articles.

1. Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation

2. DIPLOID/TRIPLOID MIXOPLOIDY AND HYPOMELANOSIS OF ITO

3. Hypomelanosis of Ito: a manifestation of mosaicism or chimerism.

4. Pigmentary dysplasias, hypomelanosis of Ito, and genetic mosaicism

Cited by 40 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. Hypomelanosis of Ito (Incontinentia Pigmenti Achromians);Neurocutaneous Disorders;2022

2. Disorders of Hypopigmentation;Harper's Textbook of Pediatric Dermatology;2019-11-20

3. Pigmentary mosaicism: a review of original literature and recommendations for future handling;Orphanet Journal of Rare Diseases;2018-03-05

4. Hypomelanosis of Ito;Atlas of Genetic Diagnosis and Counseling;2017

5. Hypomelanosis of Ito;Atlas of Genetic Diagnosis and Counseling;2016

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