Molecular diagnosis of a novel heterozygous 268C?T (R90C) mutation inTGIF gene in a fetus with holoprosencephaly and premaxillary agenesis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference19 articles.
1. A Novel Homeobox Protein Which Recognizes a TGT Core and Functionally Interferes with a Retinoid-responsive Motif
2. Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired
3. Prenatal diagnosis of partial monosomy 18p(18p11.2?pter) and trisomy 21q(21q22.3?qter) with alobar holoprosencephaly and premaxillary agenesis
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5. Further evidence for complex inheritance of holoprosencephaly: Lessons learned from pre‐ and postnatal diagnostic testing in Germany;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2018-06
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