(Q35202068)

7 August 2017

Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases (English)

1 reference

7 August 2017

Prader–Willi syndrome

1 reference

Ledbetter DH

1

1 reference

7 August 2017

Mascarello JT

2

1 reference

7 August 2017

Riccardi VM

3

1 reference

7 August 2017

Harper VD

4

1 reference

7 August 2017

Airhart SD

5

1 reference

7 August 2017

Strobel RJ

6

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 March 1982

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

34

1 reference

7 August 2017

278-285

1 reference

7 August 2017

2

1 reference

A girl with the Prader-Willi syndrome and Robertsonian translocation 45,XX,t(14;15)(p11;q11) which was present in three normal family members

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Deletions of chromosome 15 as a cause of the Prader-Willi syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

A new case of rearrangement of chromosome 15 associated with Prader Willi syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Localization of heterochromatin in human chromosomes.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

High Resolution of Human Chromosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Mental retardation associated with "balanced" chromosome rearrangements

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Systematic analysis of 95 reciprocal translocations of autosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Quantitative analysis of high-resolution trypsin-giemsa bands on human prometaphase chromosomes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

De novo 13q paracentric inversion in a boy with cleft palate and mental retardation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

The Prader-Willi syndrome with a 15/3 translocation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

The Prader-Willi syndrome and 15-15 translocation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Modification of DAPI banding on human chromosomes by prestaining with a DNA-binding oligopeptide antibiotic, distamycin A.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

15/15 translocation in Prader-Willi syndrome

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

Visualization of nucleolar organizer regions in mammalian chromosomes using silver staining

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1685279

A case of Prader-Willi syndrome in a girl with a small extra chromosome

28 July 2018

1 reference

12 December 2020

[Staining of human chromosomes with acridine orange after treatment with 5 bromodeoxyuridine]

1 reference

12 December 2020

Prader-Willi syndrome and chromosomal mosaicism 46,XY/47,XY,+mar in two cases

1 reference

12 December 2020

Prader-Willi syndrome and a bisatellited derivative of chromosome 15

1 reference

12 December 2020

Chromosomal abnormality in Prader-Willi syndrome

1 reference

12 December 2020

An extra idic(15p)(q11) chromosome in Prader-Willi syndrome

1 reference

12 December 2020

Identifiers

PMCID

1685279

1 reference

7 August 2017

1 reference