Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency

This publication has 29 references indexed in Scilit:

• Confirmation of X-linked hypogammaglobulinemia with isolated growth hormone deficiency as a disease entity
  The Journal of Pediatrics, 1990
• Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus
  Genomics, 1990
• Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia
  Human Genetics, 1989
• Nonrandom X chromosome inactivation in B cells from carriers of X chromosome-linked severe combined immunodeficiency.
  Proceedings of the National Academy of Sciences, 1988
• Carrier detection in typical and atypical X-linked agammaglobulinemia
  The Journal of Pediatrics, 1988
• Close linkage of random DNA fragments from Xq 21.3–22 to X-linked agammaglobulinaemia (XLA)
  Human Genetics, 1987
• Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity
  Human Genetics, 1986
• Childhood common variable immunodeficiency with autoimmune disease
  The Journal of Pediatrics, 1986
• Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.
  Journal of Clinical Investigation, 1986
• X-Linked Hypogammaglobulinemia and Isolated Growth Hormone Deficiency
  New England Journal of Medicine, 1980