Clinical delineation of a patient with trisomy 12q23q24
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference29 articles.
1. A girl with partial trisomy 12q24.31 inherited from her father and a possible novel syndrome transmitted from her mother;Bao;Am. J. Med. Genet. A,2005
2. Noonan syndrome;Burgt;Orphanet J. Rare Dis.,2007
3. De novo pure 12q22q24.33 duplication: first report of a case with mental retardation, ADHD, and Dandy-Walker malformation;Cappellacci;Am. J. Med. Genet. A,2006
4. Mosaicism for duplication 12q (12q13 → q24.2) in a dysmorphic male infant;Dixon;J. Med. Genet.,1993
5. Pure direct duplication (12)(q24.1→q24.2) in a child with Marcus Gunn phenomenon and multiple congenital anomalies;Doco-Fenzy;Am. J. Med. Genet. A,2006
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3. Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter);Vojnosanitetski pregled;2020
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