Pituitary macroadenoma and cranial osteoma in a manifesting heterozygote with the Opitz G/BBB syndrome

This publication has 14 references indexed in Scilit:

• The human FXY gene is located within Xp22.3: implications for evolution of the mammalian X chromosome.
  Human Molecular Genetics, 1998
• Brain magnetic resonance imaging findings in the Opitz G/BBB syndrome: Extension of the spectrum of midline brain anomalies
  American Journal of Medical Genetics, 1993
• CNS midline anomalies in the opitz G/BBB syndrome: Report on 12 Brazilian patients
  American Journal of Medical Genetics, 1992
• Opitz (BBB/G) syndrome: Oral manifestations
  American Journal of Medical Genetics, 1992
• A girl with G syndrome and agenesis of the corpus callosum
  American Journal of Medical Genetics, 1987
• G syndrome (hypertelorism with esophageal abnormality and hypospadias, or hypospadias‐dysphagia, or “Opitz‐Frias” or “opitz‐G” syndrome)—perspective in 1987 and bibliography
  American Journal of Medical Genetics, 1987
• Incidental pituitary adenomas
  Journal of Neurosurgery, 1981
• Coloboma-hypospadias
  American Journal of Medical Genetics, 1981
• Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly—a new syndrome? Part I: Clinical, causal, and pathogenetic considerations
  American Journal of Medical Genetics, 1980
• Studies of malformation syndromes of man VB: The hypertelorism-hypospadias (BBB) syndrome
  European Journal of Nuclear Medicine and Molecular Imaging, 1977