Down syndrome (trisomy 21) with premaxillary agenesis and semilobar holoprosencephaly
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.33072/fullpdf
Reference25 articles.
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4. Prenatal diagnosis of partial trisomy 3p(3p23->pter) and monosomy 7q(7q36->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia;Chen;Prenat Diagn,1999
5. Prenatal diagnosis of de novo partial trisomy 13q (13q22 -> qter) and partial monosomy 8p (8p23.3 -> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart;Chen;Prenat Diagn,2005
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1. HOLOPROSENCEPHALY: CHROMOSOMAL ABNORMALITIES IN THE ETIOPATHOGENESIS OF 127 ANTENATAL CASES;İstanbul Tıp Fakültesi Dergisi;2021-04-16
2. Syndromes associated with holoprosencephaly;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-05-17
3. Clinical and Demographic Evaluation of a Holoprosencephaly Cohort From the Kyoto Collection of Human Embryos;The Anatomical Record;2018-04-16
4. Current World Literature;Current Opinion in Pediatrics;2010-12
5. Holoprosencephaly due to numeric chromosome abnormalities;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2010-02-15
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