Rezultati - B-M Anderlid

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  1. 1
    Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome

    Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome od María Clara Bonaglia, Roberto Giorda, Elisa Mani, Giammarco Aceti, B-M Anderlid, Anna Baroncini, Tiziano Pramparo, Orsetta Zuffardi

    Izdano 2005
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  2. 2
    Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)

    Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH) od Nicole Maas, Griet Van Buggenhout, Femke Hannes, Bernard Thienpont, Damien Sanlaville, Klaas Kok, Alina T. Midro, Joris Andrieux, B-M Anderlid, Jacqueline Schoumans, Roel Hordijk, Koenraad Devriendt, JP Fryns, Joris Vermeesch

    Izdano 2007
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