家族性易位（2号染色体长臂缺失；5号染色体短臂增加）中的重复缺失综合征 - Suppr

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Duplication deficiency syndrome in familial translocation (2q-;5p+).

作者信息

Bijlsma J B, de France H, Bleeker-Wagemakers E M

出版信息

Humangenetik. 1971;12(2):110-22. doi: 10.1007/BF00291466.

DOI:10.1007/BF00291466

PMID:5568729

Abstract

摘要

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引用本文的文献

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本文引用的文献

A human skin culture technique used for cytological examinations.

Br J Exp Pathol. 1960 Feb;41(1):31-7.

THE "CAT CRY" SYNDROME.

Am J Dis Child. 1964 Nov;108:538-42. doi: 10.1001/archpedi.1964.02090010540014.

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"Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case.

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A complex familial chromosome translocation.

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