Linkage disequilibrium and founder effect analysis of the NF1 gene in French Canadians from the Quebec population.

This publication has 21 references indexed in Scilit:

• A novel mutation in the neurofibromatosis type 1 (NF1) gene promotes skipping of two exons by preventing exon definition
  Journal of Molecular Biology, 2001
• Clouston hidrotic ectodermal dysplasia (HED): genetic homogeneity, presence of a founder effect in the French Canadian population and fine genetic mapping
  European Journal of Human Genetics, 2000
• Neurofibromatosis type 1: A model condition for the study of the molecular basis of variable expressivity in human disorders
  American Journal of Medical Genetics, 1999
• Neurofibromatosis Type 1: Piecing the Puzzle Together
  Canadian Journal of Neurological Sciences, 1998
• Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association
  American Journal of Medical Genetics, 1996
• The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac α and β myosin heavy chain genes on chromosome 14q11.2−q13
  Human Molecular Genetics, 1995
• Genomic organization of the neurofibromatosis 1 gene (NF1)
  Genomics, 1995
• Two CA/GT repeat polymorphisms in intron 27 of the human neurofibromatosis type 1 (NF1) gene
  Human Genetics, 1994
• A highly informative CA/GT repeat polymorphism in intron 38 of the human neurofibromatosis type 1 (NF1) gene
  Human Genetics, 1993
• Le déséquilibre de liaison
  médecine/sciences, 1991