A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene. (Q36762586)

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29 October 2019

title

A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene (English)

1 reference

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29 October 2019

author name string

A Mutirangura

1

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29 October 2019

A Jayakumar

2

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29 October 2019

J S Sutcliffe

3

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29 October 2019

M Nakao

4

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29 October 2019

M J McKinney

5

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29 October 2019

K Buiting

6

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29 October 2019

B Horsthemke

7

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29 October 2019

A L Beaudet

8

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29 October 2019

A C Chinault

9

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29 October 2019

D H Ledbetter

10

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29 October 2019

publication date

1 December 1993

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29 October 2019

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29 October 2019

volume

18

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29 October 2019

issue

3

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29 October 2019

page(s)

546-552

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Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents

29 October 2019

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Vector-Alu PCR: a rapid step in mapping cosmids and YACs

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Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences

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A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression

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Systematic generation of sequence-tagged sites for physical mapping of human chromosomes: Application to the mapping of human chromosome 7 using yeast artificial chromosomes

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DNA deletion and its parental origin in Angelman syndrome patients

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Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion

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FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions

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Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

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Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis

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Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region

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

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Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region

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7 January 2021

Exclusion of the GABAA-receptor beta 3 subunit gene as the Angelman's syndrome gene

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7 January 2021

A novel, rapid method for the isolation of terminal sequences from yeast artificial chromosome (YAC) clones

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7 January 2021

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7 January 2021

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Identifiers

DOI

1 reference

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29 October 2019

1 reference