Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome (Q33864953)

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

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

3953677

retrieved

29 July 2017

title

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

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Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

author name string

M G Butler

series ordinal

1

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Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

F J Meaney

series ordinal

2

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Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

C G Palmer

series ordinal

3

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Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

language of work or name

English

0 references

publication date

1 March 1986

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Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

published in

American Journal of Medical Genetics Part A

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stated in

Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

volume

23

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stated in

Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

issue

3

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Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

page(s)

793-809

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Europe PubMed Central

PubMed publication ID

3953677

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29 July 2017

cites work

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

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PubMed Central

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5 July 2018

The cytogenetic controversy in the Prader-Labhart-Willi syndrome

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PubMed Central

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5 July 2018

Prader-Willi syndrome: are there population differences?

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PubMed Central

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5 July 2018

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

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PubMed Central

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5 July 2018

Translocations in Prader-Willi syndrome.

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PubMed Central

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5 July 2018

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

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PubMed Central

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5 July 2018

Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings.

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PubMed Central

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5 July 2018

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases

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PubMed Central

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5 July 2018

Prader-Willi syndrome in black females

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PubMed Central

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5 July 2018

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

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PubMed Central

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5 July 2018

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

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PubMed Central

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5 July 2018

The Prader-Labhart-Willi syndrome: review of the literature and report of nine cases

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5 July 2018

Hypogonadotropinism in Prader-Willi syndrome. Induction of puberty and sperm altogenesis by clomiphene citrate

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5 July 2018

Hypotonia, mental retardation, obesity, and cryptorchidism associated with dwarfism and diabetes in children

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5 July 2018

Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome. A follow-up report on 38 cases.

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5 July 2018

High Resolution of Human Chromosomes

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5 July 2018

Growth, body composition, and development of obese and lean children

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5 July 2018

The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature

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5 July 2018

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

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992

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5 July 2018

Mental retardation associated with "balanced" chromosome rearrangements

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992

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5 July 2018

Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992

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5 July 2018

Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992

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5 July 2018

PRADER-WILLI SYNDROME IN BOY OF TEN WITH PREDIABETES.

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992

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29 October 2018

Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992

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29 October 2018

Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494992

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29 October 2018

Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-resolution bands in human fibroblast chromosomes induced by actinomycin D

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Parental origin of de novo chromosome rearrangements

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader--Willi syndrome associated with an interstitial deletion of chromosome 15

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Benign congenital hypotonia with chromosomal anomaly

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple reproducible method for prometaphase chromosome analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Roentgenographic Manifestations of the Prader-Willi Syndrome

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome associated with inversion of chromosome 15

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/3953677

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1002/AJMG.1320230307

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3953677

retrieved

29 July 2017

PMC publication ID

5494992

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3953677

retrieved

29 July 2017

PubMed publication ID

3953677

1 reference

stated in

Europe PubMed Central

PubMed publication ID

3953677

retrieved

29 July 2017

 

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