(Q47446101)

16 January 2018

title

Two cases of cri-du-chat syndrome with mild phenotypic effect but with different size of 5p deletion (English)

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16 January 2018

1 reference

Smith A

1

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16 January 2018

Field B

series ordinal

2

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16 January 2018

Murray R

series ordinal

3

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16 January 2018

Nelson J

series ordinal

4

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16 January 2018

publication date

1 June 1990

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16 January 2018

Journal of Paediatrics and Child Health

published in

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16 January 2018

volume

26

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16 January 2018

issue

3

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16 January 2018

page(s)

152-154

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16 January 2018

The Cri du Chat syndrome: epidemiology, cytogenetics, and clinical features

cites work

1 reference

https://api.crossref.org/works/10.1111/J.1440-1754.1990.TB02414.X

Psychomotor development in 65 home-reared children with cri-du-chat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111/J.1440-1754.1990.TB02414.X

Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111/J.1440-1754.1990.TB02414.X

Computer-assisted analysis of chromosomal abnormalities: detection of a deletion in aniridia-Wilms' tumor syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111/J.1440-1754.1990.TB02414.X

Clinical heterogeneity in 80 home-reared children with cri du chat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111/J.1440-1754.1990.TB02414.X

10.1111/J.1440-1754.1990.TB02414.X

21 January 2018

Identifiers

DOI

1 reference

16 January 2018

1 reference

16 January 2018