Importance of microdeletions of chromosomal region 22q11 as a cause of selected malformations of the ventricular outflow tracts and aortic arch: A three-year prospective study

Author:

Webber Steven A.,Hatchwell Eli,Barber John C.K.,Daubeney Piers E.F.,Crolla John A.,Salmon Anthony P.,Keeton Barry R.,Temple I.Karen,Dennis Nick R.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference31 articles.

1. Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome;Scambler;Genomics,1991

2. Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome;Carey;Am J Hum Genet,1992

3. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11;Driscoll;Am J Hum Genet,1992

4. Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis;Driscoll;J Med Genet,1993

5. Scambler PJ, Kelly D, Lindsay E, et al. Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus. Lancet 1192;339:1138–9.

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