(Q33592964)

28 July 2017

Synchrony of oculocutaneous albinism, the Prader-Willi syndrome, and a normal karyotype (English)

1 reference

28 July 2017

0 references

Prader–Willi syndrome

1 reference

based on heuristic

inferred from title

oculocutaneous albinism

1 reference

Wallis CE

1

1 reference

PubMed ID

2732995

28 July 2017

Beighton PH

series ordinal

2

1 reference

PubMed ID

2732995

28 July 2017

language of work or name

English

0 references

publication date

1 May 1989

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

26

1 reference

28 July 2017

337-339

1 reference

28 July 2017

5

1 reference

Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015603

Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi 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=1015603

Abnormalities of the central visual pathways in Prader-Willi syndrome associated with hypopigmentation.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015603

Hypopigmentation in the Prader-Willi 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=1015603

Familial oculo-cutaneous hypopigmentation of dominant transmission due to a disorder in melanocyte formation. Association of Prader-Willi syndrome with a chromosome abnormality in one of the subjects involved

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015603

Clinical comparison of 59 Prader-Willi patients with and without the 15(q12) deletion

21 June 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/2732995

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

PMCID

1015603

1 reference

28 July 2017

1 reference

PubMed ID

2732995