无脑畸形与18号染色体缺失相关。 - Suppr

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Arrhinencephaly associated with a deficiency involving chromosome 18.

作者信息

McDermott A, Insley J, Barton M E, Roowe P, Edwards J H, Cameron A H

出版信息

J Med Genet. 1968 Mar;5(1):60-7. doi: 10.1136/jmg.5.1.60.

DOI:10.1136/jmg.5.1.60

PMID:5653872

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1468608/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/228e/1468608/0e0189b3a3c6/jmedgene00376-0066-a.jpg

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本文引用的文献

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Am J Hum Genet. 1965 Sep;17(5):410-9.

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Cytogenetics. 1964;3:201-6. doi: 10.1159/000129811.

A 46 CHROMOSOME CEBOCEPHALY, WITH REMARKS ON THE RELATION OF 13-15 TRISOMY TO HOLOPROSENCEPHALY (ARHINENCEPHALY).一例46条染色体的无脑畸形，并论及13 - 15三体与前脑无裂畸形（无嗅脑畸形）的关系

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Neurology. 1963 Nov;13:913-8. doi: 10.1212/wnl.13.11.913.

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[Exclusion of certain autosomal localizations of blood and serum group genes].

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