(Q33586909)

28 July 2017

title

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

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28 July 2017

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Prader–Willi syndrome

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Hawkey CJ

1

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28 July 2017

Smithies A

series ordinal

2

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28 July 2017

language of work or name

English

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publication date

1 April 1976

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

volume

13

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28 July 2017

issue

2

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28 July 2017

page(s)

152-157

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

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

Immunoreactive insulin and growth hormone responses in patients with 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=1013377

Weight control of children with 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=1013377

Persistent hypernatremia due to abnormal thirst mechanism in a 13-year-old child with nephrogenic diabetes insipidus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

Hypogonadism due to luteotropin-releasing hormone (LHRH) deficiency in a child with Prader-Labhart-Willi syndrome (author's transl)

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

Forme fruste of the Prader-Willi syndrome (HHHO) and balanced D-E translocation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

A syndrome of benign congenital hypotonia, gross obesity, delayed intellectual development, retarded bone age, and unusual facies

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

21 June 2018

Prader-Willi syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

HYPOGENITAL DYSTROPHY WITH DIABETIC TENDENCY

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

PRADER-WILLI SYNDROME IN BOY OF TEN WITH PREDIABETES.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

Chromosomal Translocation in a Mentally Deficient Child with Cryptorchidism

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

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

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013377

Benign congenital hypotonia with chromosomal anomaly

31 October 2018

1 reference

12 December 2020

Cardiorespiratory syndrome of obesity in a child; case report and necropsy findings

1 reference

12 December 2020

Prader-Willi syndrome: report of cases

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12 December 2020

Translocation between both members of chromosome pair number 15 causing recurrent abortions

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12 December 2020

A rapid banding technique for human chromosomes

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12 December 2020

Prader-Willi-Labhart-syndrome in infancy (author's transl)

1 reference

12 December 2020

Prader-Labhart-Willi syndrome. Clinical and psychopathological findings in four patients (author's transl)

1 reference

12 December 2020

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

12 December 2020

Roentgenographic Manifestations of the Prader-Willi Syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Pathology of muscular hypotonia in the Prader-Willi syndrome. Light and electron microscopic study

1 reference

12 December 2020

The Prader-Willi syndrome

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12 December 2020

Prader-Willi syndrome

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12 December 2020

Prader-Willi syndrome

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12 December 2020

[Syndrome associated with adiposis, cryptorchism and mental retardation accompanied by a chromosomal aberration]

1 reference

12 December 2020

Identifiers

PMC publication ID

1013377

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28 July 2017

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