Prenatal diagnosis of 22q11 deletions: a series of five cases with congenital heart defects.

Author:

Raymond F L,Simpson J M,Mackie C M,Sharland G K

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference12 articles.

1. Minimum prevalence of chromosome 22ql 1 deletions;Wilson, D.I.; Cross, I.E.; Wren, C.; Scambler, P.J.; Burn, J.; Goodship, J.;Am J Hum Genet,1994

2. Prevalence of 22ql 1 microdeletion;du Montcel S, Tezenas; H, Mendizabal; S, Ayme; A, Levy; N, Philip;Jf Med Genet,1996

3. Molecular definition of the deletions in velo-cardio-facial syndrome;Morrow, B.; Goldberg, R.; Carlson, C.;Am J Hum Genet,1995

4. Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22ql 1 deletion;JO, Van Hemel; C, Schaap; D, Van Opstal; MP, Mulder; MF, Niermeijer; JHC, Meijers;J Med Genet,1995

5. Chromosome 22ql 1 microdeletions in tetralogy of Fallot;Trainer, A.H.; Morrison, N.; Dunlop, A.; Wilson, N.; Tolmie, J.;Arch Dis Child,1996

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