Increased Gene Dosage at Xq26–q27 Is Associated with X-Linked Hypopituitarism

This publication has 23 references indexed in Scilit:

• Variable X-linked recessive hypopituitarism with evidence of gonadotropin deficiency in two pre-pubertal males
  Clinical Genetics, 2008
• The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X
  Nature, 2001
• Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia
  Human Molecular Genetics, 2001
• Adrenocorticotropin Deficiency in Combined Pituitary Hormone Deficiency Patients Homozygous for a Novel PROP1 Deletion
  Journal of Clinical Endocrinology & Metabolism, 2000
• Identification and Characterization of an Xq26–q27 Duplication in a Family with Spina Bifida and Panhypopituitarism Suggests the Involvement of Two Distinct Genes
  Genomics, 2000
• The molecular basis for developmental disorders of the pituitary gland in man
  Clinical Genetics, 2000
• How many homeobox genes does it take to make a pituitary gland?
  Trends in Genetics, 1998
• Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse
  Nature Genetics, 1998
• Mutations in PROP1 cause familial combined pituitary hormone deficiency
  Nature Genetics, 1998
• Cretinism with combined hormone deficiency caused by a mutation in the PIT1 gene
  Nature Genetics, 1992