Martine Blayau


Ontology type: schema:Person     


Person Info

NAME

Martine

SURNAME

Blayau

Publications in SciGraph latest 50 shown

  • 2013-07-18 Erratum: Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-01-09 Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2010-08-18 p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-10-05 Idiopathic Gastric Acid Hypersecretion in a Patient With MUTYH-Associated Polyposis in THE AMERICAN JOURNAL OF GASTROENTEROLOGY
  • 2003-05-27 Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France in HUMAN GENETICS
  • 2002-11-21 Molecular screening of the TGIF gene in holoprosencephaly: identification of two novel mutations in HUMAN GENETICS
  • 2000-10-03 A new mutation in the six-domain of SIX3 gene causes holoprosencephaly in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 1998-11 FRAXE : the HindIII/OXE20 restriction polymorphism is not a rare variant in HUMAN GENETICS
  • 1996-11 Haemochromatosis and HLA–H in NATURE GENETICS
  • 1996-04 Identification of a novel mutation in CFTR gene exon 8 (L375F) in a CUAVD phenotype in HUMAN GENETICS
  • 1993-04 Analysis of 160 CF chromosomes: detection of a novel mutation in exon 20 in HUMAN GENETICS
  • 1992-04 Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosis in HUMAN GENETICS
  • 1990-08 HLA class I gene polymorphism in genetic hemochromatosis in HUMAN GENETICS
  • 1989-01 Ferritin H gene polymorphism in idiopathic hemochromatosis in HUMAN GENETICS
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