(Q34439719)

2 August 2017

title

A novel phenotypic pattern in X-linked inheritance: craniofrontonasal syndrome maps to Xp22. (English)

1 reference

Andrew Oliver Mungo Wilkie

2 August 2017

author

14

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2 August 2017

12

Munnich A

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2 August 2017

Feldman GJ

1

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2 August 2017

Ward DE

2

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2 August 2017

Lajeunie-Renier E

3

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2 August 2017

Saavedra D

4

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2 August 2017

Robin NH

5

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2 August 2017

Proud V

6

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2 August 2017

Robb LJ

7

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2 August 2017

Der Kaloustian V

8

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2 August 2017

Carey JC

9

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2 August 2017

Cohen MM Jr

10

1 reference

2 August 2017

Cormier V

11

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2 August 2017

Zackai EH

13

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2 August 2017

Price RA

15

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2 August 2017

Muenke M

16

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2 August 2017

publication date

1 October 1997

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2 August 2017

published in

Human Molecular Genetics

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2 August 2017

volume

6

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2 August 2017

issue

11

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2 August 2017

page(s)

1937-1941

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Fibroblast-growth-factor receptor mutations in human skeletal disorders

2 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Craniosynostosis: genes and mechanisms

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Craniofrontonasal syndrome: study of 41 patients

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Craniofrontonasal dysplasia: phenotypic expression in females and males and genetic considerations

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

An integrated YAC map of the human X chromosome

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Mutations altering the structure of epidermal growth factor-like coding sequences at the Drosophila Notch locus

21 January 2018

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https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

The Notch locus and the genetic circuitry involved in early Drosophila neurogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Functional equivalence of human X- and Y-encoded isoforms of ribosomal protein S4 consistent with a role in Turner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Mutation of HOXA13 in hand-foot-genital syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Escape from X inactivation in human and mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Delineation of the male phenotype in carniofrontonasal syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

Strategies for multilocus linkage analysis in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F6.11.1937

21 January 2018

Identifiers

DOI

10.1093/HMG/6.11.1937

1 reference

2 August 2017

1 reference