SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Scott Newman, Karen E. Hermetz, Brooke Weckselblatt, M. Katharine Rudd, Next-Generation Sequencing of Duplication CNVs Reveals that Most Are Tandem and Some Create Fusion Genes at Breakpoints, The American Journal of Human Genetics, 2015, 96, 2, 208

    CrossRef

  2. 2
    John J. Connolly, Joseph T. Glessner, Berta Almoguera, David R. Crosslin, Gail P. Jarvik, Patrick M. Sleiman, Hakon Hakonarson, Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts, Frontiers in Genetics, 2014, 5,

    CrossRef

  3. 3
    Sylvie Nguyen-Minh, Katrin Drossel, Denise Horn, Imma Rost, Birgit Spors, Angela M. Kaindl, Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy, Gene, 2013, 523, 1, 92

    CrossRef

  4. 4
    Silvana Beri, Maria Clara Bonaglia, Roberto Giorda, Low-copy repeats at the human VIPR2 gene predispose to recurrent and nonrecurrent rearrangements, European Journal of Human Genetics, 2013, 21, 7, 757

    CrossRef

  5. You have free access to this content5
    JY Hehir-Kwa, R Pfundt, JA Veltman, N de Leeuw, Pathogenic or not? Assessing the clinical relevance of copy number variants, Clinical Genetics, 2013, 84, 5