Combined Goltz and Aicardi syndromes in a terminal Xp deletion: Are they a contiguous gene syndrome?-Reference-Cited by-同舟云学术

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Combined Goltz and Aicardi syndromes in a terminal Xp deletion: Are they a contiguous gene syndrome?

Published:1992-07-15 Issue:5 Volume:43 Page:839-843
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Naritomi Kenji,Izumikawa Yoshinori,Nagataki Shigetoshi,Fukushima Yoshimitsu,Wakui Keiko,Niikawa Norio,Hirayama Kiyotake

Publisher

Wiley

Subject

Genetics (clinical)

Reference19 articles.

1. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

2. Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.

3. Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.

4. Karyotyp-Phenotyp-Lorrelation bei einem 46,Xdel(X)(p22)-Befund

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