(Q41813418)

12 October 2017

The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis (English)

1 reference

12 October 2017

De Vries BB

1

1 reference

12 October 2017

Niermeijer MF

series ordinal

2

1 reference

12 October 2017

language of work or name

English

0 references

publication date

1 October 1994

1 reference

Journal of Medical Genetics

12 October 2017

1 reference

12 October 2017

31

1 reference

12 October 2017

10

1 reference

12 October 2017

820

1 reference

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype

12 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050136

PubMed Central

reference URL

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050136

PubMed Central

reference URL

27 July 2018

Identifiers

DOI

10.1136/JMG.31.10.820

1 reference

12 October 2017

1 reference

12 October 2017

PubMed publication ID

7837263

1 reference