Literature DB >> 21912441

Molecular diagnosis and treatment of two x-linked disorders.

Cyril Mamotte1.   

Abstract

Year:  2011        PMID： 21912441      PMCID： PMC3157947     

Source DB:  PubMed          Journal:  Clin Biochem Rev        ISSN： 0159-8090


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  6 in total

1.  Newborn screening.

Authors:  James J Pitt
Journal:  Clin Biochem Rev       Date:  2010-05

Review 2.  Review of Duchenne muscular dystrophy (DMD) for the pediatricians in the community.

Authors:  Sumit Verma; Yaacov Anziska; Joan Cracco
Journal:  Clin Pediatr (Phila)       Date:  2010-08-19       Impact factor: 1.168

3.  Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.

Authors:  I Oberlé; F Rousseau; D Heitz; C Kretz; D Devys; A Hanauer; J Boué; M F Bertheas; J L Mandel
Journal:  Science       Date:  1991-05-24       Impact factor: 47.728

Review 4.  Duchenne muscular dystrophy: issues in expanding newborn screening.

Authors:  Alex R Kemper; Melissa A Wake
Journal:  Curr Opin Pediatr       Date:  2007-12       Impact factor: 2.856

5.  Screening newborn infants for Duchenne muscular dystrophy.

Authors:  J E Bowman
Journal:  BMJ       Date:  1993-02-06

6.  Experience with screening newborns for Duchenne muscular dystrophy in Wales.

Authors:  D M Bradley; E P Parsons; A J Clarke
Journal:  BMJ       Date:  1993-02-06
  6 in total

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