Medical genetics: advances in brief: Familial case with sequence variant in the testis-determining region associated with two sex phenotypes

Samankaltaisia teoksia

• Familial case with sequence variant in the testis-determining region associated with two sex phenotypes.
  Tekijä: Vilain, E, et al.
  Julkaistu: (1992)
• Medical genetics: advances in brief
  Tekijä: Goodship, Judith
  Julkaistu: (1992)
• Medical genetics: advances in brief: Recombination of 4p16 DNA markers in an unusual family with Huntington disease
  Tekijä: Goodship, Judith
  Julkaistu: (1992)
• Medical genetics: advances in brief: Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion
  Tekijä: Goodship, Judith
  Julkaistu: (1992)
• Medical genetics: advances in brief: Girls with fragile X syndrome: physical and neurocognitive status and outcome
  Tekijä: Goodship, Judith
  Julkaistu: (1992)