Literature DB >> 16222674

A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP).

Liesbeth Spruijt1, Pieter Verdyck, Wim Van Hul, Wim Wuyts, Christine de Die-Smulders.   

Abstract

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Year:  2005        PMID： 16222674     DOI： 10.1002/ajmg.a.30923

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  4 in total

Review 1.  Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology.

Authors:  Peter G Farlie; Naomi L Baker; Patrick Yap; Tiong Y Tan
Journal:  Mol Syndromol       Date:  2016-10-29

2.  ALX4 gain-of-function mutations in nonsyndromic craniosynostosis.

Authors:  Garima Yagnik; Apar Ghuman; Sundon Kim; Christina G Stevens; Virginia Kimonis; Joan Stoler; Pedro A Sanchez-Lara; Jonathan A Bernstein; Cyril Naydenov; Hicham Drissi; Michael L Cunningham; Jinoh Kim; Simeon A Boyadjiev
Journal:  Hum Mutat       Date:  2012-08-13       Impact factor: 4.878

3.  A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.

Authors:  Cristina M Justice; Garima Yagnik; Yoonhee Kim; Inga Peter; Ethylin Wang Jabs; Monica Erazo; Xiaoqian Ye; Edmond Ainehsazan; Lisong Shi; Michael L Cunningham; Virginia Kimonis; Tony Roscioli; Steven A Wall; Andrew O M Wilkie; Joan Stoler; Joan T Richtsmeier; Yann Heuzé; Pedro A Sanchez-Lara; Michael F Buckley; Charlotte M Druschel; James L Mills; Michele Caggana; Paul A Romitti; Denise M Kay; Craig Senders; Peter J Taub; Ophir D Klein; James Boggan; Marike Zwienenberg-Lee; Cyrill Naydenov; Jinoh Kim; Alexander F Wilson; Simeon A Boyadjiev
Journal:  Nat Genet       Date:  2012-11-18       Impact factor: 38.330

Review 4.  Genetic advances in craniosynostosis.

Authors:  Wanda Lattanzi; Marta Barba; Lorena Di Pietro; Simeon A Boyadjiev
Journal:  Am J Med Genet A       Date:  2017-02-04       Impact factor: 2.802
  4 in total

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