One case of 2q37 deletion syndrome clinical and genetic diagnosis

One case of 2q37 deletion syndrome : clinical and genetic diagnosis

OBJECTIVE: To diagnose a new born baby with 2q37 deletion syndrome by comprehensive use of cytogenetic and molecular techniques and to investigate the phenotype characteristics and applicability of array-comparative genomic hybridization (array-CGH) and multiplex ligation-dependent probe amplificati...

Ausführliche Beschreibung

Bibliographische Detailangaben
Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 51(2013), 12 vom: 03. Dez., Seite 934-7
1. Verfasser: Geng, Qian (VerfasserIn)
Weitere Verfasser: Xie, Jian-sheng, Wu, Wei-qing, Luo, Fu-wei, Chen, Wu-bin
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2013
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:Case Reports English Abstract Journal Article Research Support, Non-U.S. Gov't