与4号和5号染色体短臂部分缺失相关的综合征群的比较。 - Suppr | 超能文献

A comparison of the syneromes associated with a partial deletion of the short arms of chromosomes number 4 and number 5.

作者信息

Falk K

出版信息

Mt Sinai J Med. 1970 Jan-Feb;37(1):60-6.

Abstract

摘要

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A comparison of the syneromes associated with a partial deletion of the short arms of chromosomes number 4 and number 5.与4号和5号染色体短臂部分缺失相关的综合征群的比较。

Mt Sinai J Med. 1970 Jan-Feb;37(1):60-6.

2

Cri-du-chat syndrome in a 10 year old girl with deletion of the short arms of chromosome number 5. Observations on dermatoglyphics, maxillo-mandibular measurements and sound spectrograms.一名10岁患有5号染色体短臂缺失的女孩的猫叫综合征。关于皮纹学、上颌下颌测量及声谱图的观察

Helv Paediatr Acta. 1967 Apr;22(1):2-12.

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"Cri du chat" syndrome. Partial deletion of the short arm of a chromosome No. 5. Report of a case.“猫叫综合征”。5号染色体短臂部分缺失。病例报告。

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[Partial deletion of the short branch of chromosome 5 (a new case: Pathological Anatomy Week, October 1965)].5号染色体短臂部分缺失（一个新病例：1965年10月病理解剖周）

Ann Pediatr (Paris). 1967 Nov 2;14(11):783.

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Deletion of the short arm of chromosome 5 from a subject with cri-du-chat syndrome respository identification no. GM-71.来自一名患有猫叫综合征（存储编号GM - 71）的受试者的5号染色体短臂缺失。

Cytogenet Cell Genet. 1976;17(4):239-40. doi: 10.1159/000130718.

6

[Symposium. Autoradiographical studies on human chromosome replication. 3. Autoradiographic and measurement studies of group B chromosomes in five patients with a Bp-chromosome].

Jinrui Idengaku Zasshi. 1969 Dec;14(3):222-3.

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[Mental retardation in the crying cat syndrome. Comparison of the intellectual level in the partial deletion of the short arm of chromosome 5 with trisomy 21 and deletions of chromosome 18. Apropos of 118 cases taken from the literature].[猫叫综合征中的智力迟钝。5号染色体短臂部分缺失与21三体及18号染色体缺失患者智力水平的比较。基于文献中的118例病例]

Rev Neuropsychiatr Infant. 1968 Mar;16(3):257-67.

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[A case of crying cat syndrome. Clinical and genetic study].[一例猫叫综合征。临床与遗传学研究]

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[Partial deletion of the short arm of chromosome 4 (Wolf's syndrome). Two further cases].[4号染色体短臂部分缺失（沃尔夫综合征）。另外两例]

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[Partial deletion of short arms in chromosomes from group B with translocation to group D in the father of children with multiple developmental anomalies].[B组染色体短臂部分缺失并向D组易位，见于患有多种发育异常儿童的父亲]

Pol Tyg Lek. 1969 Dec 1;24(48):1845-8.

引用本文的文献

1

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features.猫叫综合征：流行病学、细胞遗传学及临床特征

Hum Genet. 1978 Nov 16;44(3):227-75. doi: 10.1007/BF00394291.