The Coffin-Lowry syndrome (Q33676721)

28 July 2017

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title

The Coffin-Lowry syndrome (English)

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28 July 2017

main subject

Coffin-Lowry syndrome

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Young ID

1

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28 July 2017

language of work or name

English

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publication date

1 May 1988

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

25

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28 July 2017

issue

5

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28 July 2017

page(s)

344-348

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Brief clinical report: early recognition of the Coffin-Lowry syndrome

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050463

The Coffin-Lowry syndrome. A study of two new index patients and their families

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050463

A new dominant gene mental retardation syndrome. Association with small stature, tapering fingers, characteristic facies, and possible hydrocephalus.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050463

Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's 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=1050463

Coffin-Lowry syndrome and schizophrenia: a family 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=1050463

The Coffin-Lowry syndrome: a facio digital mental retardation 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=1050463

The Coffin-Lowry syndrome: an inherited faciodigital mental retardation 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=1050463

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050463

The Coffin-Lowry syndrome. Experience from four centres.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050463

[The coffin, Siris, Wegienka syndrome]

30 October 2018

1 reference

12 December 2020

The syndrome of Coffin, Siris and Wegienka: report of a case

1 reference

12 December 2020

Coffin-Lowry syndrome in an Afro-American family

1 reference

12 December 2020

Orodental findings and genetic disorders

1 reference

12 December 2020

Abnormal proteodermatan sulfate in three patients with Coffin-Lowry syndrome

1 reference

12 December 2020

Forearm fullness in Coffin-Lowry syndrome: a misleading yet possible early diagnostic clue

1 reference

12 December 2020

Identifiers

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28 July 2017

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