Microdeletions of chromosomal region 22q11 in patients with congenital conotruncal cardiac defects.

Author:

Goldmuntz E,Driscoll D,Budarf M L,Zackai E H,McDonald-McGinn D M,Biegel J A,Emanuel B S

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Familial risk of congenital heart disease assessed in a population based epidemiology study;Boughman, J.A.; Berg, K.A.; Astemborski, J.A.;AmJ7 Med Genet,1987

2. Update on counseling the family with a first-degree relative with a congenital heart defect;Nora, J.J.; Nora, A.H.;Am 7 Med Genet,1988

3. Maternal transmission of congenital heart diseases: new recurrence risk figures and the auestions of cytoplasmic inheritance and vulnerability to teratogens;Nora, J.J.; Nora, A.H.;Am J Cardiol,1987

4. The spectrum of DiGeorge syndrome;Conley, M.E.; Beckwith, J.B.; Mancer, J.F.K.; Tenckhoff, I.,1979

5. Cardiac malformations in the velo-cardio-facial;Young, D.; Shprintzen, R.J.; Goldberg, R.B.,1980

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