Sotos syndrome common deletion is mediated by directly oriented subunits within inverted Sos-REP low-copy repeats

By Kurotaki Naohiro  

Human Molecular Genetics, Vol. 14, Iss. 4, 2005-02 ,pp. : 535-542

Oxford University Press

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Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage

By Jones Christopher   Müllenbach Roman   Grossfeld Paul  

Human Molecular Genetics, Vol. 9, Iss. 8, 2000-05 ,pp. : 1201-1208

Oxford University Press

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Frequent translocations occur between low copy repeats on chromosome 22q11.2 (LCR22s) and telomeric bands of partner chromosomes

By Shimizu N.  

Human Molecular Genetics, Vol. 12, Iss. 15, 2003-08 ,pp. : 1823-1837

Oxford University Press

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Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis

By Shaikh Tamim H.  

Human Molecular Genetics, Vol. 9, Iss. 4, 2000-03 ,pp. : 489-501

Oxford University Press

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The Drosophila Developmental Gene Fat Facets Has a Human Homologue in Xp11.4 Which Escapes X-inactivation and Has Related Sequences on Yq11.2

By Jones Michael H.   Furlong Robert A.   Burkin Heather   Jennifer Chalmers I.   Brown Graeme M.   Khwaja Omar   Affara Nabeel A.  

Human Molecular Genetics, Vol. 5, Iss. 11, 1996-11 ,pp. : 1695-1701

Oxford University Press

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