PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

This publication has 17 references indexed in Scilit:

• Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy
  Nucleic Acids Research, 1985
• Structure and Expression of a Complementary DNA for the Nuclear Coded Precursor of Human Mitochondrial Ornithine Transcarbamylase
  Science, 1984
• Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome
  Human Genetics, 1984
• FIRST TRIMESTER CHROMOSOMAL ANALYSIS OF COMPLEX STRUCTURAL REARRANGEMENTS WITH RHA BANDING ON CHORIONIC VILLI
  The Lancet, 1983
• Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.
  Journal of Medical Genetics, 1983
• CARRIER DETECTION IN DUCHENNE MUSCULAR DYSTROPHY BY USE OF CLONED DNA SEQUENCES
  The Lancet, 1983
• Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome
  Nucleic Acids Research, 1983
• Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy
  Nature, 1982
• Regional localization on the human X of DNA segments cloned from flow sorted chromosomes
  Nucleic Acids Research, 1982
• The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1969