Prenatal Diagnosis and Molecular Cytogenetic Characterization of De Novo Partial Trisomy 7p (7p15.3→pter) and Partial Monosomy 13q (13q33.3→qter) Associated With Dandy-Walker Malformation, Abnormal Skull Development and Microcephaly

• Päätekijät: Chih-Ping Chen (Tekijä), Ming Chen (Tekijä), Yi-Ning Su (Tekijä), Fuu-Jen Tsai (Tekijä), Schu-Rern Chern (Tekijä), Chin-Yuan Hsu (Tekijä), Pei-Chen Wu (Tekijä), Dai-Dyi Town (Tekijä), Dong-Jay Lee (Tekijä), Gwo-Chin Ma (Tekijä), Wayseen Wang (Tekijä)
• Aineistotyyppi: Kirja
• Julkaistu: Elsevier, 2010-09-01T00:00:00Z.
• Aiheet: article
• Linkit: Connect to this object online.

Objective: To present the prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with Dandy-Walker malformation (DWM), abnormal skull development, microcephaly and multiple congenital anomalies. Mat...