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The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7 (Q68330563)

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scientific article published on 01 November 1991

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English	The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7	scientific article published on 01 November 1991

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

The syntenic relationship between the critical deletion region for the Prader-Willi/Angelman syndromes and proximal mouse chromosome 7 (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

chromosomal deletion syndrome

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

nucleic acid sequence homology

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

author name string

J. R. Chaillet

1

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Europe PubMed Central

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28 October 2022

J. H. Knoll

2

0000-0001-6691-1710

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

B. Horsthemke

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1685485

28 October 2022

M. Lalande

4

1 reference

Europe PubMed Central

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28 October 2022

publication date

1 November 1991

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23 September 2019

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National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1685485

28 October 2022

work available at URL

https://api.elsevier.com/content/article/PII:0888754391900902?httpAccept=text/xml

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

https://api.elsevier.com/content/article/PII:0888754391900902?httpAccept=text/plain

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

11

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

773-776

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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

2

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Parental origin of chromosome 15 deletion in Prader-Willi syndrome

3

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

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

4

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromes

7

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

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

8

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

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

9

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

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

11

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

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

12

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Identification of cDNA clones for the human microtubule-associated protein tau and chromosomal localization of the genes for tau and microtubule-associated protein 2.

13

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

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

15

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Genetic variation at a locus (TAM-1) for submaxillary gland protease in the mouse and its location on chromosome No. 7

17

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Differential imprinting and expression of maternal and paternal genomes

18

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome

19

1 reference

10.1016/0888-7543(91)90090-2

https://api.crossref.org/works/10.1016/0888-7543(91)90090-2

28 October 2022

Identifiers

10.1016/0888-7543(91)90090-2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1685485%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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