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BRCA1/BRCA2 germline mutations and chemotherapy-related hematological toxicity in breast cancer patients Friedlaender, Alex; Vuilleumier, Aurélie; Viassolo, Valeria; Ayme, Aurélie; ... Labidi-Galy, Sana Intidhar 2019
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MECP2 mutant allele in a boy with Rett syndrome and his unaffected heterozygous mother Dayer, Alexandre; Bottani, Armand; Bouchardy, Isabelle; Fluss, Joel Victor; ... Morris, Michael Andréw 2007
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Combined factor V - factor VIII deficiency (F5F8D): compound heterozygosity for two novel truncating mutations in LMAN1 in a consanguineous patient Farah, R. A.; De Moerloose, Philippe; Bouchardy, Isabelle; Morris, Michael Andréw; ... Neerman Arbez, Marguerite 2006
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Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family Neerman Arbez, Marguerite; Vu, Dung; Abu-Libdeh, Bassam; Bouchardy, Isabelle; Morris, Michael Andréw 2003
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Cystic fibrosis transmembrane conductance regulator does not affect neutrophil migration across cystic fibrosis airway epithelial monolayers Pizurki, Lara Johanna; Morris, Michael Andréw; Chanson, Marc; Solomon, Melete; ... Suter, Susanne 2000