The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region (Q67514407)

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scientific article published on 01 January 1992

Language	Label	Description	Also known as
English	The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region	scientific article published on 01 January 1992

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

The p locus is closely linked to the mouse homolog of a gene from the Prader-Willi chromosomal region (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

author name string

Y. Nakatsu

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1347469

16 September 2022

Y. Gondo

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1347469

16 September 2022

M. H. Brilliant

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1347469

16 September 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1347469

16 September 2022

publication date

1 January 1992

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

number of pages

3

1 reference

based on heuristic

inferred from page(s)

Mammalian Genome

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

69-71

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal origin of 15q11-13 deletions in Angelman syndrome suggests a role for genomic imprinting.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Direct Molecular Identification of the Mouse Pink-Eyed Unstable Mutation by Genome Scanning

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR)

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrence risk in the Angelman ("happy puppet") syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypopigmentation in the Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Statistical considerations for linkage analysis using recombinant inbred strains and backcrosses

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequences homologous to glutamic acid decarboxylase cDNA are present on mouse chromosomes 2 and 10.

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis of Angelman syndrome in infants

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Visual evoked potentials in Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The tyrosinase-positive oculocutaneous albinism locus is not linked to the beta-globin locus in man

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome imprinting phenomena on mouse chromosome 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/1347469

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00570442

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1347469%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

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