Chorion villus sampling in X-linked genetic disorders

This publication has 21 references indexed in Scilit:

• Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies.
  Journal of Medical Genetics, 1986
• A de novo X;13 translocation with abnormal phenotype.
  Journal of Medical Genetics, 1986
• Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis
  Clinical Genetics, 1985
• Molecular genetics of the human X chromosome.
  Journal of Medical Genetics, 1985
• Detection and sequence of mutations in the factor VIII gene of haemophiliacs
  Nature, 1985
• First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250 cases.
  Journal of Medical Genetics, 1985
• Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences
  Human Genetics, 1984
• Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28
  Nature, 1984
• The use of cloned Y chromosome-specific DNA probes for fetal sex determination in first trimester prenatal diagnosis
  Human Genetics, 1984
• CHARACTERISATION AND USE OF AN INTRAGENIC POLYMORPHIC MARKER FOR DETECTION OF CARRIERS OF HAEMOPHILIA B (FACTOR IX DEFICIENCY)
  The Lancet, 1984