Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Author:

Burn J,Takao A,Wilson D,Cross I,Momma K,Wadey R,Scambler P,Goodship J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference5 articles.

1. Deletions and microdeletions of 22ql 1.2 in velo-cardio-facial syndrome;Driscoll, D.A.; Spinner, N.B.; Budarf, M.L.;Am Med Genet,1992

2. Deletions within chromosome 22qll in familial congenital heart disease;Wilson, D.I.; Goodship, J.A.; Burn, J.; Cross, I.E.; Scambler, P.J.;Lancet,1992

3. Cardiovascular malformations in the conotruncal anomaly face syndrome;Takao, A.; Terai, M.; Ando, M.; Momma, K.,1985

4. A prospective cytogenetic study of 36 cases of DiGeorge syndrome;Wilson, D.I.; Cross, I.E.; Goodship, J.A.;Am Hum Genet,1992

5. Syndrome of the month. DiGeorge syndrome: part of CATCH 22;Wilson, D.I.; Burn, J.; Scambler, P.; Goodship, J.;Med Genet,1993

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