Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes

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American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2664-2673

John Wiley & Sons Inc

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High-resolution mapping identifies a commonly amplified 11q13.3 region containing multiple genes flanked by segmental duplications

By Gibcus Johan   Kok Klaas   Menkema Lorian   Hermsen Mario   Mastik Mirjam   Kluin Philip   Wal Jacqueline   Schuuring Ed  

Human Genetics, Vol. 121, Iss. 2, 2007-04 ,pp. : 187-201

Springer Publishing Company

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Supernumerary chromosomes, segmental duplications, and evolution

By Trifonov V.   Dementyeva P.   Beklemisheva V.   Yudkin D.   Vorobieva N.   Graphodatsky A.  

Russian Journal of Genetics, Vol. 46, Iss. 9, 2010-09 ,pp. : 1094-1096

MAIK Nauka/Interperiodica

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Familial Hypomagnesemia Maps to Chromosome 9q, not to the X Chromosome: Genetic Linkage Mapping and Analysis of a Balanced Translocation Breakpoint

By Walder R.Y.   Shalev H.   Brennan T.M.H.   Carmi R.   Elbedour K.   Scott D.A.   Hanauer A.   Mark A.L.   Patil S.   Stone E.M.   Sheffield V.C.  

Human Molecular Genetics, Vol. 6, Iss. 9, 1997-01 ,pp. : 1491-1497

Oxford University Press

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Allele-specific expression analysis by RNA-FISH demonstrates preferential maternal expression of UBE3A and imprint maintenance within 15q11– q13 duplications

By Herzing L.B.K.  

Human Molecular Genetics, Vol. 11, Iss. 15, 2002-07 ,pp. : 1707-1718

Oxford University Press

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