Prenatal diagnosis of holoprosencephaly
Author:
Affiliation:
1. Division of NeurologyChildren's National Health SystemWashington DC
2. Division of Fetal and Transitional MedicineChildren's National Health SystemWashington DC
3. Division of RadiologyChildren's National Health SystemWashington DC
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.c.31618
Reference62 articles.
1. Middle interhemispheric fusion: An unusual variant of holoprosencephaly;Barkovich A. J.;American Journal of Neuroradiology,1993
2. Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly
3. Molecular evaluation of foetuses with holoprosencephaly shows high incidence of microdeletions in the HPE genes
4. Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype
5. Sonoembryology and early prenatal diagnosis of neural anomalies
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