Literature DB >> 11343324

Jackson-Weiss syndrome.

M M Cohen.   

Abstract

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Year:  2001        PMID： 11343324     DOI： 10.1002/ajmg.1271

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  5 in total

1.  Genomic screening of fibroblast growth-factor receptor 2 reveals a wide spectrum of mutations in patients with syndromic craniosynostosis.

Authors:  Shih-hsin Kan; Navaratnam Elanko; David Johnson; Laura Cornejo-Roldan; Jackie Cook; Elsa W Reich; Susan Tomkins; Alain Verloes; Stephen R F Twigg; Sahan Rannan-Eliya; Donna M McDonald-McGinn; Elaine H Zackai; Steven A Wall; Maximilian Muenke; Andrew O M Wilkie
Journal:  Am J Hum Genet       Date:  2002-01-04       Impact factor: 11.025

2.  Severe craniolacunae and upper and lower extremity anomalies resulting from Crouzon syndrome, FGFR2 mutation, and Ser347Cys variant.

Authors:  Cassio Eduardo Raposo-Amaral; Yuri Moresco Oliveira; Rafael Denadai; Cesar Augusto Raposo-Amaral; Enrico Ghizoni
Journal:  Childs Nerv Syst       Date:  2021-01-06       Impact factor: 1.475

3.  Apert syndrome: report of a case with emphasis on oral manifestations.

Authors:  B Vadiati Saberi; A Shakoorpour
Journal:  J Dent (Tehran)       Date:  2011-06-30

4.  Craniosynostosis genetics: The mystery unfolds.

Authors:  Inusha Panigrahi
Journal:  Indian J Hum Genet       Date:  2011-05

5.  Molecular Analysis of Twist1 and FGF Receptors in a Rabbit Model of Craniosynostosis: Likely Exclusion as the Loci of Origin.

Authors:  Phillip H Gallo; James J Cray; Emily L Durham; Mark P Mooney; Gregory M Cooper; Sandeep Kathju
Journal:  Int J Genomics       Date:  2013-05-08       Impact factor: 2.326
  5 in total

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