Should the 3C (craniocerebellocardiac) syndrome be included in the spectrum of velocardiofacial syndrome and DiGeorge sequence?

Author:

Butler M G,Mowrey P

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference7 articles.

1. Cerebellar atrophy in a patient with velocardiofacial syndrome;Lynch, D.R.; McDonald-McGinn, D.M.; Zackai, E.H.;J Med Genet,1995

2. Atrioventricular canal and 3C (cranio-cerebellocardiac) syndrome;Digilio, M.C.; Marino, B.; Giannotti, A.;Am J Med Genet,1995

3. Dandy-Walker (like) malformation, atrioventricular septal defect and a similar pattern of minor anomalies in 2 sisters: a new syndrome?;A, Ritscher D.Schinzel; E, Bolthauser; J, Briner; U, Arbenz; P, Sigg;Am J Med Genet,1987

4. 3C syndrome: third occurrence of cranio-cerebello-cardiac dysplasia (RitscherSchinzel syndrome);Verloes, A.; Dreese, M.F.; Jovanovic, M.; Dodinval, P.; Geubelle, F.;Clin Genet,1989

5. 3C syndrome: another case;Mims, L.R.C.; Say, B.;Clin Genet,1989

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Genetic variation in the 22q11 locus and susceptibility to schizophrenia;Proceedings of the National Academy of Sciences;2002-12-11

2. Absence of a del(22q11) in a patient with the 3C (craniocerebellocardiac) syndrome.;Journal of Medical Genetics;1998-04-01

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