(Q52090855)

English

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

scientific article published in December 1984

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

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

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

author name string

M Haspeslagh

1

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

J P Fryns

2

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

L Beusen

3

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

F Van Dessel

4

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

L Vinken

5

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

E Moens

6

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

H Van den Berghe

7

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

publication date

1 December 1984

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

European Journal of Pediatrics

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

143

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

82-86

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

2

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

https://scigraph.springernature.com/pub.10.1007/bf00445790

0 references

Metacarpophalangeal pattern profiles in the evaluation of skeletal malformations.

1 reference

https://api.crossref.org/works/10.1007%2FBF00445790

21 January 2018

A New Dominant Gene Mental Retardation Syndrome

1 reference

https://api.crossref.org/works/10.1007%2FBF00445790

21 January 2018

Fragile sites on human chromosomes: demonstration of their dependence on the type of tissue culture medium

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation, abnormal fingers, and skeletal anomalies: Coffin's syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The coffin, Siris, Wegienka syndrome]

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Coffin-Lowry syndrome. Experience from four centres.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation without physical abnormality (Renpenning's syndrome) in sibs in an institution.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Coffin-Lowry syndrome in an Afro-American family

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Coffin syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A marker X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Coffin-Lowry syndrome: a simply inherited trait comprising mental retardation, faciodigital anomalies and skeletal involvement

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal proteodermatan sulfate in three patients with Coffin-Lowry syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/6519116

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00445790

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/6519116

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