Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: Prenatal and postnatal late replication studies-Reference-Cited by-同舟云学术

Preaxial acrofacial dysostosis (Nager syndrome) associated with an inherited and apparently balanced X;9 translocation: Prenatal and postnatal late replication studies

Published:1993-06-01 Issue:4 Volume:46 Page:379-383
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zori Roberto T.,Gray Brian A.,Bent-Williams Angela,Driscoll Daniel J.,Williams Charles A.,Zackowski Joleen L.

Publisher

Wiley

Subject

Genetics(clinical)

Reference10 articles.

1. Nager acrofacial dysostosis

2. Autosomal recessive inheritance of Nager acrofacial dysostosis.

3. X-inactivation patterns in lymphocytes and skin fibroblasts of three cases of X-autosome translocations with abnormal phenotypes

4. Possible inactivation of part of chromosome 13 due to 13qXp translocation associated with retinoblastoma

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