X-linked myotubular myopathy: a linkage study

Author:

Darnfors Catarina,Larsson H. E. Börje,Oldfors Anders,Kyllerman Mårten,Gustavson Karl-Henrik,Bjursell Gunnar,Wahlström Jan

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Anonymous X-chromosomal probes revealing DNA polymorphisms one of which is a deletion of more than 3 kb;Ahrens;Cytogenet. Cell Genet.,1986

2. A strategy to reveal high-frequency RFLPs along the X-chromosome;Aldridge;Am. J. Hum. Genet.,1984

3. Construction of a genetic linkage map in man using restriction fragment length polymorphisms;Botstein;Am. J. Hum. Genet.,1980

4. Molecular analysis of the human X-chromosome;Bruns;Cytogenet. Cell Genet. (HGM7),1984

5. Report of the committee on methods of linkage analysis and reporting;Conneally;Cytogenet. Cell Genet. (HGM8),1985

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2. Congenital (Structural) Myopathies;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

3. Centronuclear (myotubular) myopathy;Orphanet Journal of Rare Diseases;2008-09-25

4. X-Linked Myotubular Myopathy: Report of a Case With Novel Mutation;Journal of Child Neurology;2007-04

5. X-Linked Myotubular and Centronuclear Myopathies;Journal of Neuropathology & Experimental Neurology;2005-07

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