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The atrioventricular canal defect is the congenital heart disease connecting short rib‐polydactyly and oral‐facial‐digital syndromes

The atrioventricular canal defect is the congenital heart disease connecting short... References Adetoro OO , Komolafe F , Anjorin A ( 1984 ): Hydrolethalus syndrome in consecutive African siblings . Pediatr Radiol 14 : 422 – 424 . Akoun R , Bagard M ( 1956 ): Le maladie d'Ellis‐van Creveld . Algérie Méd 60 : 769 – 772 . Amati F , Mari A , Mingarelli R , Gennarelli M , Digilio MC , Giannotti A , Marino B , Novelli G , Dallapiccola B ( 1995 ): Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region 8p . Am J Med Genet 57 : 483 – 488 . Camera G , Marasini M , Pozzolo S , Camera A ( 1994 ): Oral‐facial‐digital syndrome: Report on a transitional type between the Mohr and Váradi syndromes in a fetus . Am J Med Genet 53 : 196 – 198 . Carmi R , Boughman JA , Ferencz C ( 1992 ): Endocardial cushion defect: Further studies of “isolated” versus “syndromic” occurrence . Am J Med Genet 43 : 569 – 575 . Chitayat D , Hahm SYE , Marion RW , Sachs GS , Goldman D , Hutcheon RG , Weiss R , Cho http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png American Journal of Medical Genetics Part A Wiley

The atrioventricular canal defect is the congenital heart disease connecting short rib‐polydactyly and oral‐facial‐digital syndromes

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References (31)

Publisher
Wiley
Copyright
Copyright © 1997 Wiley Subscription Services, Inc., A Wiley Company
ISSN
1552-4825
eISSN
1552-4833
DOI
10.1002/(SICI)1096-8628(19970110)68:1<110::AID-AJMG25>3.0.CO;2-W
Publisher site
See Article on Publisher Site

Abstract

References Adetoro OO , Komolafe F , Anjorin A ( 1984 ): Hydrolethalus syndrome in consecutive African siblings . Pediatr Radiol 14 : 422 – 424 . Akoun R , Bagard M ( 1956 ): Le maladie d'Ellis‐van Creveld . Algérie Méd 60 : 769 – 772 . Amati F , Mari A , Mingarelli R , Gennarelli M , Digilio MC , Giannotti A , Marino B , Novelli G , Dallapiccola B ( 1995 ): Two pedigrees of autosomal dominant atrioventricular canal defect (AVCD): Exclusion from the critical region 8p . Am J Med Genet 57 : 483 – 488 . Camera G , Marasini M , Pozzolo S , Camera A ( 1994 ): Oral‐facial‐digital syndrome: Report on a transitional type between the Mohr and Váradi syndromes in a fetus . Am J Med Genet 53 : 196 – 198 . Carmi R , Boughman JA , Ferencz C ( 1992 ): Endocardial cushion defect: Further studies of “isolated” versus “syndromic” occurrence . Am J Med Genet 43 : 569 – 575 . Chitayat D , Hahm SYE , Marion RW , Sachs GS , Goldman D , Hutcheon RG , Weiss R , Cho

Journal

American Journal of Medical Genetics Part AWiley

Published: Oct 10, 1997

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