Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome
References (27)
The face and immune system in tetralogy of Fallot
Int. J. Cardiol
(1989)- et al.
Localization of 27 DNA markers to the region of human chromosome pter-22q11 deleted in patients with the DiGeorge syndrome and duplicated in the der22 syndrome
Genomics
(1990) - et al.
The spectrum of the DiGeorge syndrome
J. Pediatr
(1979) - et al.
A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity
Anal. Biochem
(1983) - et al.
Confirmation of autosomal dominant transmission of the DiGeorge malformation complex
J. Pediatr
(1988) - et al.
Toward a long-range map of human chromosomal band 22q11
Genomics
(1989) - et al.
Chemically induced congenital thymic dysgenesis in the rat: A model of the DiGeorge syndrome
Clin. Immunol. Immunopathol
(1983) - et al.
Facial and immunological anomalies associated with tetralogy of Fallot
Int. J. Cardiol
(1989) - et al.
Familial third-fourth pharyngeal pouch syndrome with apparent autosomal dominant transmission
J. Pediatr
(1984) - et al.
DiGeorge syndrome and 22q11 rearrangements
Hum. Genet
(1986)
Dependence of thymus development on derivatives of the neural crest
Science
(1984)
A deletion in chromosome 22 can cause DiGeorge syndrome
Hum. Genet
(1981)
Molecular cytogenetics: Toward dissection of the contiguous gene syndromes
Am. J. Hum. Genet
(1988)
Cited by (0)
- 1
Current address: Green College, Oxford, UK.
Copyright © 1991 Published by Elsevier Inc.