Autosomal recessive alobar holoprosencephaly with essentially normal faces-Reference-Cited by-同舟云学术

Autosomal recessive alobar holoprosencephaly with essentially normal faces

Published:2002-09-15 Issue:1 Volume:112 Page:28-30
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Barr Mason,Cohen M. Michael

Publisher

Wiley

Subject

Genetics(clinical)

Reference9 articles.

1. Holoprosencephaly in infants of diabetic mothers

2. Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

3. Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities

4. 1969. Genetic considerations in a sibship of cyclopia and clefts. In: editors. The clinical delineation of birth defects: part II, malformation syndrome. New York: Alan R. Liss, for the National Foundation-March of Dimes. BD:OAS. V(2):p 113-118.

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2. A rare case of alobar holoprosencephaly with normal facies;Journal of Pediatric Neurosciences;2022

3. Middle interhemispheric variant of holoprosencephaly: First prenatal report of a ZIC2 missense mutation;Clinical Case Reports;2020-04-30

4. Lobar holoprosencephaly with craniofacial defects in a Friesian calf: A case report;Veterinary Medicine and Science;2020-01-23

5. Holoprosencephaly, orofacial cleft, and frontonaso‐orbital encephaloceles: Genetic evaluation of a possible new syndrome;American Journal of Medical Genetics Part A;2019-07-28