(Q34687154)

3 August 2017

1 reference

title

Tapetoretinal degeneration in brothers with apparent Cohen syndrome: nosology with Mirhosseini-Holmes-Walton syndrome (English)

1 reference

3 August 2017

Tapetoretinal degeneration in brothers with apparent Cohen syndrome: Nosology with Mirhosseini-Holmes-Walton syndrome (English)

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

22 November 2022

1 reference

1 reference

O. Steinlein

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1785634

22 November 2022

G. Tariverdian

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1785634

22 November 2022

H. U. Boll

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1785634

22 November 2022

F. Vogel

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1785634

22 November 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1785634

22 November 2022

publication date

1 November 1991

1 reference

full work available at URL

3 August 2017

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320410213

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320410213

22 November 2022

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

American Journal of Medical Genetics Part A

22 November 2022

published in

1 reference

3 August 2017

41

1 reference

3 August 2017

2

1 reference

3 August 2017

196-200

1 reference

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

3 August 2017

1

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

Confirmation of the Cohen syndrome

22 November 2022

2

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

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

22 November 2022

3

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

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

22 November 2022

4

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

Cohen syndrome: further delineation and inheritance

22 November 2022

5

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

The syndrome of retinal pigmentary degeneration, microcephaly, and severe mental retardation (Mirhosseini-Holmes-Walton syndrome): report of two patients

22 November 2022

6

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

Syndrome of pigmentary retinal degeneration, cataract, microcephaly, and severe mental retardation

22 November 2022

7

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

Are the Mirhosseini-Holmes-Walton syndrome and the Cohen syndrome identical?

22 November 2022

9

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

The clinical features of the Cohen syndrome: further case reports

22 November 2022

10

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

Cardiac involvement in the Cohen syndrome: a case report.

22 November 2022

11

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320410213

22 November 2022

Identifiers

1 reference

3 August 2017

1 reference