Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome

This publication has 32 references indexed in Scilit:

• Localization of 27 DNA markers to the region of human chromosome 22q11-pter deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome
  Genomics, 1990
• The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus
  Genomics, 1990
• Features of Turner's and DiGeorge's syndromes in a child with an X;22 translocation.
  Journal of Medical Genetics, 1989
• A subfamily of alphoid repetitive DNA shared by the nor-bearing human chromosomes 14 and 22
  Genomics, 1988
• Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11).
  Journal of Medical Genetics, 1987
• Hypoparathyroidism and T cell immune defect in a patient with 10p deletion syndrome
  The Journal of Pediatrics, 1986
• Cardiovascular anomalies in digeorge syndrome and importance of neural crest as a possible pathogenetic factor
  Published by Elsevier ,1986
• Dispersed human immunoglobulin κ light-chain genes
  Nature, 1986
• The spectrum of the DiGeorge syndrome
  The Journal of Pediatrics, 1979
• A link between Turner syndrome in the male and Turner syndrome in the female with normal chromosomes
  The Journal of Pediatrics, 1965