One case of 2q37 deletion syndrome clinical and genetic diagnosis

von Geng, Qian
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2013)

Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization

von Zhu, Chun-jiang
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2012)

Mutation of thyroid peroxidase gene in 35 patients with congenital hypothyroidism

von Li, Hai-fei
Veröffentlicht in: Zhonghua er ke za zhi = Chinese journal of pediatrics (2011)