Literature DB >> 16763963

A new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis.

Anne Donzel-Javouhey, Christel Thauvin-Robinet, Veronica Cusin, Nathalie Madinier, Eric Manceau, Dominique Dipanda, Véronique Dulieu, Francine Mugneret, Frédéric Huet, Jean-Raymond Teyssier, Laurence Faivre.   

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Year:  2006        PMID： 16763963     DOI： 10.1002/ajmg.a.31314

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


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  3 in total

1.  The array of clinical phenotypes of males with mutations in Methyl-CpG binding protein 2.

Authors:  Jeffrey L Neul; Timothy A Benke; Eric D Marsh; Steven A Skinner; Jonathan Merritt; David N Lieberman; Shannon Standridge; Timothy Feyma; Peter Heydemann; Sarika Peters; Robin Ryther; Mary Jones; Bernhard Suter; Walter E Kaufmann; Daniel G Glaze; Alan K Percy
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2018-12-07       Impact factor: 3.568

2.  Genetic Approach to Diagnosis of Intellectual Disability.

Authors:  Ratna Dua Puri; Moni Tuteja; I C Verma
Journal:  Indian J Pediatr       Date:  2016-09-13       Impact factor: 1.967

Review 3.  MECP2 mutations in males.

Authors:  Laurent Villard
Journal:  J Med Genet       Date:  2007-03-09       Impact factor: 6.318
  3 in total

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