X Chromosome Inactivation in Carriers of Barth Syndrome

Author:

Ørstavik Karen Helene,Ørstavik Ragnhild E.,Naumova Anna K.,D'Adamo Patrizia,Gedeon Agi,Bolhuis Pieter A.,Barth Peter G.,Toniolo Daniela

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. An X chromosome gene regulates hematopoietic stem cell kinetics;Abkowitz;Proc Natl Acad Sci USA,1998

2. Barth syndrome: clinical features and confirmation of gene localisation to distal Xq28;Adès;Am J Med Genet,1993

3. Application of carrier testing to genetic counseling for X-linked agammaglobulinemia;Allen;Am J Hum Genet,1994

4. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am J Hum Genet,1992

5. An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes;Barth;J Neurol Sci,1983

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