Related content

Understanding Mesenchymal Cancer: The Liposarcoma-Associated t(12;16) (q13;;p11) Chromosomal Translocation as a Model

By  

Current Genomics, Vol. 3, Iss. 4, 2002-08 ,pp. : 237-244

Bentham Science Publishers

Access to resources Recommend Favorite

A YAC contig encompassing the 11q14.3 breakpoint of a translocation associated with schizophrenia, and including the tyrosinase gene

By Petit Joëlle   Boisseau Pierre   Taine Laurence   Gauthier Bruno   Arveiler Benoit  

Mammalian Genome, Vol. 10, Iss. 6, 1999-06 ,pp. : 649-652

Springer Publishing Company

Access to resources Recommend Favorite

Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A

By  

Molecular Syndromology, Vol. 1, Iss. 3, 2010-09 ,pp. : 113-120

Karger

Access to resources Recommend Favorite

Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment

By Schneider Eberhard   Mrker Tina   Daser Angelika   Frey-Mahn Gabriele   Beyer Vera   Farcas Ruxandra   Schneider-Rtzke Brigitte   Kohlschmidt Nicolai   Grossmann Brbel   Bauss Katharina   Napiontek Ulrike   Keilmann Annerose   Bartsch Oliver   Zechner Ulrich   Wolfrum Uwe   Haaf Thomas  

Human Molecular Genetics, Vol. 18, Iss. 4, 2009-02 ,pp. : 655-666

Oxford University Press

Access to resources Recommend Favorite

Pathology and nuclear abnormalities in hearts of transgenic mice expressing M371K lamin A encoded by an LMNA mutation causing Emery–Dreifuss muscular dystrophy

By Wang Yuexia   Herron Alan J.   Worman Howard J.  

Human Molecular Genetics, Vol. 15, Iss. 16, 2006-08 ,pp. : 2479-2489

Oxford University Press

Access to resources Recommend Favorite