(Q41575180)

4 October 2017

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title

Mental retardation in Nance-Horan syndrome: clinical and neuropsychological assessment in four families (English)

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4 October 2017

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1

Toutain A

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4 October 2017

Ayrault AD

2

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4 October 2017

Moraine C

series ordinal

3

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4 October 2017

publication date

1 August 1997

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American Journal of Medical Genetics Part A

4 October 2017

published in

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4 October 2017

volume

71

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4 October 2017

issue

3

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4 October 2017

page(s)

305-314

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X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12.

4 October 2017

cites work

1 reference

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Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

21 January 2018

1 reference

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Validation of the Revised Behavior Summarized Evaluation Scale.

21 January 2018

1 reference

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The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females

21 January 2018

1 reference

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The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule

21 January 2018

1 reference

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Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.

21 January 2018

1 reference

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Localization of non-specific X-linked mental retardation genes

21 January 2018

1 reference

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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

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21 January 2018

XLMR genes: update 1996.

1 reference

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

21 January 2018

1 reference

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Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

21 January 2018

1 reference

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A high resolution deletion map of human chromosome Xp22.

21 January 2018

1 reference

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Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region.

21 January 2018

1 reference

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

21 January 2018

1 reference

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XNP mutation in a large family with Juberg-Marsidi syndrome

21 January 2018

1 reference

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21 January 2018

The Nance-Horan syndrome

1 reference

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Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819970822%2971%3A3%3C305%3A%3AAID-AJMG11%3E3.0.CO%3B2-O

10.1002/(SICI)1096-8628(19970822)71:3<305::AID-AJMG11>3.0.CO;2-O

21 January 2018

Identifiers

DOI

1 reference

4 October 2017

1 reference