Le syndrome X fragile est encore méconnu: efficacité du diagnostic moléculaire chez les proposants avec retard mental

This publication has 18 references indexed in Scilit:

• The impact of genetic counselling on females in fragile X families.
  Journal of Medical Genetics, 1994
• Fragile‐X syndrome in North East Essex: towards systematic screening: clinical selection
  Journal of Intellectual Disability Research, 1994
• Cytogenetic versus DNA diagnosis in routine referrais for fragile X syndrome
  The Lancet, 1993
• Population studies of the fragile X: a molecular approach.
  Journal of Medical Genetics, 1993
• Population screening for fragile X
  The Lancet, 1992
• On some technical aspects of direct DNA diagnosis of the fragile X syndrome
  American Journal of Medical Genetics, 1992
• Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
  Cell, 1991
• Clinical screening score for the fragile X (Martin‐Bell) syndrome
  American Journal of Medical Genetics, 1991
• Further segregation analysis of the fragile X syndrome with special reference to transmitting males
  Human Genetics, 1985
• FEASIBILITY OF FRAGILE X CHROMOSOME PRENATAL DIAGNOSIS DEMONSTRATED
  The Lancet, 1981