Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome-Reference-Cited by-同舟云学术

Interstitial deletion 9q22.32-q33.2 associated with additional familial translocation t(9;17)(q34.11;p11.2) in a patient with Gorlin-Goltz syndrome and features of Nail-Patella syndrome

Published:2003-06-13 Issue:2 Volume:124A Page:179-191
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Midro Alina T.,Panasiuk Barbara,Tümer Zeynep,Stankiewicz Paweł,Silahtaroglu Asli,Lupski James R.,Zemanova Zuzana,Stasiewicz-Jarocka Beata,Hubert Ewa,Tarasów Eugeniusz,Famulski Waldemar,Zadrożna-Tołwińska Barbara,Wasilewska Ewa,Kirchhoff Marie,Kalscheuer Vera,Michalova Kyra,Tommerup Niels

Funder

Polish grant of Medical University Białystok

Czech

Deutches Bundesministerium für Bildung, Wissenschaft, Forschung und Technologie

Nationales Genomforschungsnetz-Umweltbedingte Erkranungen

EU-Commission

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference42 articles.

1. A report of a child with a deletion (9)(q34.3): A recognisable phenotype?;Ayyash;J Med Genet,1997