Work

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

Year: 2003

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.20367

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

Institutions: Medical University of Białystok, University of Copenhagen, Baylor College of Medicine, Texas Children's Hospital, General University Hospital in Prague, Copenhagen University Hospital, Max Planck Institute for Molecular Genetics

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Danmarks Grundforskningsfond

OpenAlex ID: W1995464611

FWCI: 1.78

Cites: 40

Cited by: 42

Related to: 10