(Q34150637)

31 July 2017

title

Craniosynostosis in Alagille syndrome (English)

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31 July 2017

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Binita M Kamath

1

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31 July 2017

Catherine Stolle

2

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31 July 2017

Lynn Bason

3

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31 July 2017

Raymond P Colliton

4

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31 July 2017

David A Piccoli

5

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31 July 2017

Nancy B Spinner

6

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31 July 2017

Ian D Krantz

7

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31 July 2017

publication date

1 October 2002

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American Journal of Medical Genetics Part A

31 July 2017

published in

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31 July 2017

volume

112

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31 July 2017

issue

2

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31 July 2017

page(s)

176-180

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Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromes

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Craniosynostoses: phenotypic/molecular correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Features of Alagille syndrome in 92 patients: frequency and relation to prognosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Localization of putative stem cells in dental epithelium and their association with Notch and FGF signaling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Spectrum and frequency of jagged1 (JAG1) mutations in Alagille syndrome patients and their families

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Clinical and molecular genetics of Alagille syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

Genetic study of nonsyndromic coronal craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10608

21 January 2018

Identifiers

DOI

10.1002/AJMG.10608

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31 July 2017

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