(Q33671915)

28 July 2017

title

The clinical features of the Cohen syndrome: further case reports (English)

1 reference

28 July 2017

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1 reference

3

Baraitser M

1 reference

28 July 2017

North C

1

1 reference

28 July 2017

Patton MA

series ordinal

2

1 reference

28 July 2017

Winter RM

series ordinal

4

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28 July 2017

language of work or name

English

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publication date

1 April 1985

1 reference

Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

22

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28 July 2017

issue

2

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28 July 2017

page(s)

131-134

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

28 July 2017

1 reference

Cohen syndrome: further delineation and inheritance

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

The Cohen syndrome: report of five new cases and a review of the literature.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

Mental retardation, hypotonia, obesity, ocular, facial, dental, and limb abnormalities (Cohen syndrome). Report of three patients

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

The Cohen syndrome: clinical and endocrinological studies of two new cases.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

Further delineation of the Cohen syndrome; report on chorioretinal dystrophy, leukopenia and consanguinity

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

Confirmation of the Cohen syndrome

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

Cardiac involvement in the Cohen syndrome: a case report.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1049398

Sexual development in a girl with Cohen syndrome

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3989828

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Cohen syndrome, an autosomal recessive disease? (author's transl)]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/3989828

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

0 references

1 reference

28 July 2017

1 reference