Absence of a del(22q11) in a patient with the 3C (craniocerebellocardiac) syndrome.

Author:

Saraiva J M,Matoso E,Marques I

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference20 articles.

1. Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?;Butler, M.G.; Mowrey, P.;JMed Genet,1996

2. First report of glaucoma as a feature of the 3C syndrome;Saraiva, J.M.; Gama, E.; Pires, M.M.; Sequeira, J.F.;Clin Dysmorphol,1995

3. Mendelian inheritance in man: catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick, V.A.,1994

4. Atrioventricular canal and 3C (cranio-cerebello-cardiac) syndrome;Digilio, M.C.; Marino, B.; Giannotti, A.; Mingarelli, R.; Dallapiccola, B.;Am J Med Genet,1995

5. Evidence for Ritscher-Schinzel syndrome in Canadian native indians;Marles, S.L.; Chodirker, B.N.; Greenberg, C.R.; Chudley, A.E.;Am J Med Genet,1995

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