Growth hormone deficiency and empty sella syndrome in a boy with dup(x)(q13.3→q21.2)

This publication has 11 references indexed in Scilit:

• Insertional translocation into the X chromosome of a 46, XY male
  Clinical Genetics, 2008
• Duplications of the X chromosome in males: evidence that most parts of the X chromosome can be active in two copies
  Human Genetics, 1991
• A new syndrome with mental retardation, short stature and an Xq duplication
  American Journal of Medical Genetics, 1988
• An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region
  Human Genetics, 1987
• Regional localization of the phosphoglycerate kinase gene and pseudogene on the human X chromosome and assignment of a related DNA sequence to chromosome 19
  Human Genetics, 1985
• Inherited tandem duplication dup(X) (q131‐q212) in a male proband
  Clinical Genetics, 1985
• Pituitary abnormalities detected by high resolution computed tomography with thin slices in primary hypothyroidism and Turner syndrome
  European Journal of Pediatrics, 1984
• Pituitary Function in the Empty Sella Syndrome
  Neuroendocrinology, 1981
• Tandem duplication dup(X)(q13q22) in a male proband inherited from the mother showing mosaicism of X-inactivation
  Human Genetics, 1980
• Accumulation of Early Mitotic Cells in Ethidium Bromide-Treated Human Lymphocyte Cultures
  Proceedings of the Japan Academy, Series B, 1979