Prader-Willi syndrome. (Q52066710)

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2 October 2019

review article

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title

Prader-Willi syndrome (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json

2 October 2019

author name string

Cassidy SB

series ordinal

1

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2 October 2019

Ledbetter DH

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json

2 October 2019

publication date

1 February 1989

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2 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json

2 October 2019

volume

7

1 reference

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2 October 2019

issue

1

1 reference

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2 October 2019

page(s)

37-54

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

2 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Recurrence risk in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Prader-Willi syndrome. Variable severity and recurrence risk

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Deletions of proximal 15q without Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Adults with Prader-Willi syndrome: a survey of 232 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Clinical heterogeneity associated with deletions in the long arm of chromosome 15: report of 3 new cases and their possible genetic significance.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

The cytogenetic controversy in the Prader-Labhart-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Identification of inverted duplicated #15 chromosomes using bivariate flow cytometric analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Linear growth response to exogenous growth hormone in Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Familial Prader-Willi syndrome with apparently normal chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Is Angelman syndrome an alternate result of del(15)(q11q13)?

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Paternal hydrocarbon exposure in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Emotional symptoms in Prader-Willi syndrome adolescents.

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

High Resolution of Human Chromosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

Characteristics of abnormal food-intake patterns in children with Prader-Willi syndrome and study of effects of naloxone

1 reference

https://api.crossref.org/works/10.1016%2FS0733-8619%2818%2930827-2

7 January 2021

10.1016/S0733-8619(18)30827-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2646521%20AND%20SRC:MED&resulttype=core&format=json

2 October 2019

1 reference