Lischner HW, Dacou C, DiGeorge AM.Normal lymphocyte transfer(NLT) test: negative response in a patient with congenital absence of the thymus[J].Transplantation, 1967,5(3): 555-557.
[2]
Saitta SC, Harris SE, Gaeth AP, et al.Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion [J].Hum Mol Genet, 2004, 13(4): 417-428.
[3]
Botto LD, May K, Fernhoff PM, et al.A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population [J].Pediatrics, 2003, 112(1 Pt 1): 101-107.
[4]
Swillen A, Devriendt K, Vantrappen G, et al.Familial deletions of chromosome 22q11: the Leuven experience[J].Am J Med Genet, 1998, 80(5): 531-532.
3.0.CO;2-L target="_blank">
[5]
Gilmour DF, Downey LM, Sheridan E, et al.Familial exudative vitreoretinopathy and DiGeorge syndrome: a new locus for familial exudative vitreoretinopathy on chromosome 22q11.2?[J].Ophthalmology, 2009, 116(8): 1522-1524.
[6]
Ryan AK, Goodship JA, Wilson DI, et al.Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study[J].J Med Genet, 1997,34(10): 798-804.