Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome

This publication has 9 references indexed in Scilit:

• Familial DiGeorge syndrome and associated partial monosomy of chromosome 22
  Human Genetics, 1984
• DiGeorge's Syndrome in Monozygotic Twins
  American Journal of Diseases of Children, 1983
• Partial monosomy of chromosome 10 short arms.
  Journal of Medical Genetics, 1983
• The association of the DiGeorge anomalad with partial monosomy of chromosome 22
  The Journal of Pediatrics, 1982
• Radioimmunoassay for the Middle Region of Human Parathyroid Hormone Using an Homologous Antiserum with a Carboxy-Terminal Fragment of Bovine Parathyroid Hormone as Radioligand*
  Journal of Clinical Endocrinology & Metabolism, 1982
• A deletion in chromosome 22 can cause digeorge syndrome
  Human Genetics, 1981
• A child trisomic for the distal part of chromosome 14q.
  Archives of Disease in Childhood, 1980
• The spectrum of the DiGeorge syndrome
  The Journal of Pediatrics, 1979
• The Human Rosette-Forming Cell as a Marker of a Population of Thymus-Derived Cells
  Journal of Clinical Investigation, 1972