Craniosynostosis: Another feature of the 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Craniosynostosis: Another feature of the 22q11.2 deletion syndrome

Published:2005 Issue:4 Volume:136A Page:358-362
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

McDonald-McGinn Donna M.,Gripp Karen W.,Kirschner Richard E.,Maisenbacher Melissa K.,Hustead Virginia,Schauer Galen M.,Keppler-Noreuil Kim M.,Ciprero Karen L.,Pasquariello Patrick,LaRossa Don,Bartlett Scott P.,Whitaker Linton A.,Zackai Elaine H.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference36 articles.

1. Identification of a patient with Bernard-Soulier syndrome and a deletion in the DiGeorge/Velo-cardio-facial chromosomal region in 22q11.2

2. Craniosynostoses: Phenotypic/molecular correlations

3. Craniosynostosis and chromosome 22q11 deletion.

4. Renal and urological tract malformations caused by a 22q11 deletion.

5. A link between Turner syndrome in the male and Turner syndrome in the female with normal chromosomes

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