Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination

By Bouche P.  

Human Molecular Genetics, Vol. 7, Iss. 1, 1998-01 ,pp. : 141-148

Oxford University Press

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Duplications of the AZFa region of the human Y chromosome are mediated by homologous recombination between HERVs and are compatible with male fertility

By Bosch E.   Jobling M.A.  

Human Molecular Genetics, Vol. 12, Iss. 3, 2003-02 ,pp. : 341-347

Oxford University Press

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WHSC1 , a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf–Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma

By Stec I.  

Human Molecular Genetics, Vol. 7, Iss. 7, 1998-07 ,pp. : 1071-1082

Oxford University Press

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A mutation in the human heme A:farnesyltransferase gene ( COX10 ) causes cytochrome c oxidase deficiency

By Valnot Isabelle   von Kleist-Retzow Jürgen-Christoph   Barrientos Antoni  

Human Molecular Genetics, Vol. 9, Iss. 8, 2000-05 ,pp. : 1245-1249

Oxford University Press

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Two long homologous retroviral sequence blocks in proximal Yq11 cause AZFa microdeletions as a result of intrachromosomal recombination events

By Kamp Christine   Hirschmann Peter   Voss Hartmut   Huellen Karin   Vogt PeterH.  

Human Molecular Genetics, Vol. 9, Iss. 17, 2000-10 ,pp. : 2563-2572

Oxford University Press

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