Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

مواد مشابهة

• Independent De Novo 22q11.2 Deletions in First Cousins With DiGeorge/Velocardiofacial Syndrome
  بواسطة: Saitta, Sulagna C., وآخرون
  منشور في: (2004)
• Increased Prevalence of Immunoglobulin A Deficiency in Patients with the Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
  بواسطة: Smith, Christopher A., وآخرون
  منشور في: (1998)
• Secondary Immunologic Consequences in Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
  بواسطة: Zemble, R., وآخرون
  منشور في: (2010)
• A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.
  بواسطة: Driscoll, D A, وآخرون
  منشور في: (1992)
• Longitudinal Analysis of Lymphocyte Function and Numbers in the First Year of Life in Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
  بواسطة: Sullivan, Kathleen E., وآخرون
  منشور في: (1999)