Molecular genetic analysis of the Prader-Willi syndrome by using fluorescent multiplex PCR of the dinucleotide repeats on chromosome 15q11-q13 (Q74492772)

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scientific article published on 01 March 1998

Language	Label	Description	Also known as
English	Molecular genetic analysis of the Prader-Willi syndrome by using fluorescent multiplex PCR of the dinucleotide repeats on chromosome 15q11-q13	scientific article published on 01 March 1998

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scholarly article

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11 November 2019

Molecular genetic analysis of the Prader-Willi syndrome by using fluorescent multiplex PCR of the dinucleotide repeats on chromosome 15q11-q13 (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9564560%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

Prader–Willi syndrome

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M J Lee

1

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11 November 2019

H Nishio

2

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11 November 2019

T Nagai

3

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11 November 2019

N Okamoto

4

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11 November 2019

T Yuki

5

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11 November 2019

K Sumino

6

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11 November 2019

publication date

1 March 1998

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11 November 2019

Clinica Chimica Acta

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11 November 2019

271

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11 November 2019

1

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11 November 2019

89-96

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11 November 2019

Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Prader-Willi syndrome: current understanding of cause and diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

DNA methylation patterns in human tissues of uniparental origin using a zinc-finger gene (ZNF127) from the Angelman/Prader-Willi region

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Maternal imprinting of human SNRPN, a gene deleted in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

The Angelman syndrome candidate gene, UBE3A/E6-AP, is imprinted in brain

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Prader-Willi Syndrome after age 15 years

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

The 1993-94 Généthon human genetic linkage map

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2897%2900238-6

7 January 2021

Identifiers

10.1016/S0009-8981(97)00238-6

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9564560%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9564560%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

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