A chromosome survey of 1062 mentally retarded patients. Evaluation of a long-term study at the Rinnekoti institution, Finland.

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作者信息

Gripenberg U, Hongell K, Knuutila S, Kähkönen M, Leisti J

出版信息

Hereditas. 1980;92(2):223-8. doi: 10.1111/j.1601-5223.1980.tb01700.x.

DOI:10.1111/j.1601-5223.1980.tb01700.x

PMID:6446531

Abstract

摘要

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引用本文的文献

A cytogenetic study of a population of mentally retarded males with special reference to the marker (X) syndrome.一项针对智障男性群体的细胞遗传学研究，特别涉及标记（X）综合征。

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Trisomy 21q: 46,XX,21s+/47,XX,+21q-(q22----qter) mosaicism (de novo) in a Down syndrome child.21号染色体长臂三体：一名唐氏综合征患儿存在46,XX,21s+/47,XX,+21q-(q22----qter)嵌合体（新发）。

Indian J Pediatr. 1984 May-Jun;51(410):363-6. doi: 10.1007/BF02754689.

A cytogenetic study of a population of retarded females with special reference to the fragile (X) syndrome.一项针对智力发育迟缓女性群体的细胞遗传学研究，特别关注脆性X综合征。

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A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome.台湾智障学童的细胞遗传学研究——特别关注脆性X染色体

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