18号染色体长臂缺失（q12.2q21.1）的嵌合体及正常细胞系的产前诊断 - Suppr

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超能文献

Prenatal diagnosis of mosaicism for del(18)(q12.2q21.1) and a normal cell line.

作者信息

Wilson M G, Lin M S

机构信息

Department of Pediatrics, University of Southern California School of Medicine, Los Angeles.

出版信息

J Med Genet. 1988 Sep;25(9):635-6. doi: 10.1136/jmg.25.9.635.

DOI:10.1136/jmg.25.9.635

PMID:3184145

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1051545/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e3b/1051545/4366ba1c43c9/jmedgene00071-0059-a.jpg

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本文引用的文献

[PARTIAL DELETION OF THE LONG ARMS OF THE CHROMOSOME 18].[18号染色体长臂部分缺失]

Pathol Biol. 1964 May;12:579-82.

United States survey on chromosome mosaicism and pseudomosaicism in prenatal diagnosis.美国产前诊断中染色体嵌合现象和假嵌合现象的调查。

Prenat Diagn. 1984 Spring;4 Spec No:97-130. doi: 10.1002/pd.1970040708.

Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].与18号染色体长臂缺失相关的综合征[del(18q)]

Am J Med Genet. 1979;3(2):155-74. doi: 10.1002/ajmg.1320030207.

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