(Q24540161)

6 July 2017

title

Mapping of a new SGBS locus to chromosome Xp22 in a family with a severe form of Simpson-Golabi-Behmel syndrome (English)

1 reference

Simpson-Golabi-Behmel syndrome

6 July 2017

main subject

1 reference

L M Brzustowicz

1

1 reference

6 July 2017

S Farrell

series ordinal

2

1 reference

6 July 2017

M B Khan

series ordinal

3

1 reference

6 July 2017

R Weksberg

series ordinal

4

1 reference

6 July 2017

language of work or name

English

0 references

publication date

1 September 1999

1 reference

American Journal of Human Genetics

6 July 2017

published in

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6 July 2017

volume

65

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6 July 2017

issue

3

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6 July 2017

page(s)

779-783

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Glypican 3 and glypican 4 are juxtaposed in Xq26.1

6 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=1377986

GPC4, the gene for human K-glypican, flanks GPC3 on xq26: deletion of the GPC3-GPC4 gene cluster in one family with Simpson-Golabi-Behmel syndrome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

A comprehensive genetic map of the human genome based on 5,264 microsatellites

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Strategies for multilocus linkage analysis in humans

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Overgrowth syndromes and genomic imprinting: from mouse to man

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Mapping of Simpson-Golabi-Behmel syndrome to Xq25-q27

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Faster sequential genetic linkage computations

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

The Golabi-Rosen syndrome--report of a second family

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Gene for Simpson-Golabi-Behmel syndrome is linked to HPRT in Xq26 in two European families

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

Avoiding recomputation in linkage analysis.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377986

A previously unrecognized X-linked syndrome of dysmorphia

29 November 2018

1 reference

12 December 2020

Simpson-Golabi-Behmel syndrome: follow-up of the Michigan family

1 reference

12 December 2020

An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3–Xp21.3

1 reference

12 December 2020

Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis

1 reference

12 December 2020

Clinical and molecular aspects of the Simpson-Golabi-Behmel syndrome

1 reference

12 December 2020

Developmental Biology: Frontiers for Clinical Genetics: Overgrowth syndromes and genomie imprinting: from mouse to man

1 reference

Crossref

https://api.crossref.org/works/10.1086%2F302527

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1086/302527

1 reference

6 July 2017

1 reference

6 July 2017

1 reference