Deletion of 9p associated with gonadal dysfunction in 46,XY but not in 46,XX human fetuses

J Med Genet. 2002 Jul;39(7):514-8. doi: 10.1136/jmg.39.7.514.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Abnormalities, Multiple / diagnosis
  • Abnormalities, Multiple / genetics
  • Abortion, Therapeutic / methods
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 9 / genetics*
  • Disorders of Sex Development
  • Female
  • Fetus / chemistry*
  • Fetus / physiology*
  • Genitalia / abnormalities
  • Gestational Age
  • Gonadal Dysgenesis, 46,XX / diagnosis
  • Gonadal Dysgenesis, 46,XX / genetics*
  • Gonadal Dysgenesis, 46,XY / diagnosis
  • Gonadal Dysgenesis, 46,XY / genetics*
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Male
  • Pregnancy
  • Pregnancy Trimester, Second
  • Prenatal Diagnosis
  • Telomere / genetics
  • Testis / chemistry
  • Testis / physiology