(Q34869864)

5 August 2017

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title

FG syndrome: linkage analysis in two families supporting a new gene localization at Xp22.3 [FGS3]. (English)

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5 August 2017

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4

John M Opitz

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5 August 2017

Sabine Dessay

1

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5 August 2017

Marie Pierre Moizard

2

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5 August 2017

Jean Louis Gilardi

3

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5 August 2017

Helen Middleton-Price

5

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5 August 2017

Marcus Pembrey

6

1 reference

5 August 2017

Claude Moraine

7

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5 August 2017

Sylvain Briault

8

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5 August 2017

publication date

1 September 2002

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American Journal of Medical Genetics Part A

5 August 2017

published in

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5 August 2017

volume

112

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5 August 2017

issue

1

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5 August 2017

page(s)

6-11

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The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability

5 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

A novel murine PKA-related protein kinase involved in neuronal differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element-binding protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Paracentric inversion of the X chromosome [inv(X)(q12q28)] in familial FG syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

MECP2 is highly mutated in X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Mapping of a gene for non-specific X linked mental retardation: evidence for linkage to chromosomal region Xp21.1-Xp22.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Strategies for multilocus linkage analysis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Localization of a gene for X-linked nonspecific mental retardation (MRX24) in Xp22.2-p22.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Studies of malformation syndromes of man XXXIII: The FG syndrome. An X-linked recessive syndrome of multiple congenital anomalies and mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

FG syndrome update 1988: note of 5 new patients and bibliography

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

XNP mutation in a large family with Juberg-Marsidi syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10546

21 January 2018

Identifiers

DOI

10.1002/AJMG.10546

1 reference

5 August 2017

1 reference