(Q39346054)

11 September 2017

Visual capacity and Prader-Willi syndrome (English)

1 reference

11 September 2017

4

I D Feurer

1 reference

11 September 2017

R Fox

1

1 reference

11 September 2017

R B Sinatra

series ordinal

2

1 reference

11 September 2017

M A Mooney

series ordinal

3

1 reference

11 September 2017

M G Butler

series ordinal

5

1 reference

11 September 2017

language of work or name

1 reference

1 November 1999

1 reference

Journal of Pediatric Ophthalmology and Strabismus

11 September 2017

1 reference

11 September 2017

36

1 reference

11 September 2017

6

1 reference

11 September 2017

331-336

1 reference

Methylation PCR analysis of Prader-Willi syndrome, Angelman syndrome, and control subjects

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

Stereopsis in human infants

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

The Prader-Willi syndrome: a study of 40 patients and a review of the literature

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

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

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

Ophthalmologic Features of Prader-Willi Syndrome

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

Prader-Willi syndrome: current understanding of cause and diagnosis

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

Methylation-specific PCR simplifies imprinting analysis

11 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

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

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5167472

17 June 2018

Prader-Willi syndrome

1 reference

12 December 2020

Stereopsis in normal infants and infants with congenital esotropia

1 reference

12 December 2020

Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P allele

1 reference

12 December 2020

Clinical correlates of chromosome 15 deletions and maternal disomy in Prader-Willi syndrome

1 reference

12 December 2020

Visual evoked potentials in Prader-Willi syndrome

1 reference

12 December 2020

Ocular findings and visual evoked potential response in the Prader-Willi syndrome

1 reference

12 December 2020

Identifiers

1 reference

11 September 2017

PubMed publication ID

11132665

1 reference