Search Results - "LEISINK, Martijn A. R"

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  1. 1
    Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation

    Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisation by KOOLEN, David A, REARDON, William, VELTMAN, Joris A, DE VRIES, Bert B. A, ROSSER, Elisabeth M, LACOMBE, Didier, HURST, Jane A, LAW, Caroline J, BONGERS, Ernie M. H. F, VAN RAVENSWAAIJ-ARTS, Conny M, LEISINK, Martijn A. R, GEURTS VAN KESSEL, Ad

    Published in European journal of human genetics : EJHG (01-09-2005)
    “…The 22q13 deletion syndrome is associated with global developmental delay, absent or delayed speech, and generalised hypotonia. In this study, the size and…”
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    The cluster variation method for efficient linkage analysis on extended pedigrees

    The cluster variation method for efficient linkage analysis on extended pedigrees by Albers, Cornelis A, Leisink, Martijn A R, Kappen, Hilbert J

    Published in BMC bioinformatics (20-03-2006)
    “…Computing exact multipoint LOD scores for extended pedigrees rapidly becomes infeasible as the number of markers and untyped individuals increase. When markers…”
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