Literature DB >> 7989049

Exclusion of linkage with chromosome 21 in families with recurrence of non-Down's atrioventricular canal.

M Gennarelli, G Novelli, M C Digilio, A Giannotti, B Marino, B Dallapiccola.   

Abstract

Entities:  

Mesh：

Year:  1994        PMID： 7989049     DOI： 10.1007/BF00206969

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


× No keyword cloud information.
  12 in total

1.  A second-generation linkage map of the human genome.

Authors:  J Weissenbach; G Gyapay; C Dib; A Vignal; J Morissette; P Millasseau; G Vaysseix; M Lathrop
Journal:  Nature       Date:  1992-10-29       Impact factor: 49.962

2.  Prevalence of left-sided obstructive lesions in patients with atrioventricular canal without Down's syndrome.

Authors:  L De Biase; V Di Ciommo; L Ballerini; M Bevilacqua; C Marcelletti; B Marino
Journal:  J Thorac Cardiovasc Surg       Date:  1986-03       Impact factor: 5.209

Review 3.  Atrioventricular canal and 8p- syndrome.

Authors:  M C Digilio; A Giannotti; B Marino; B Dallapiccola
Journal:  Am J Med Genet       Date:  1993-09-01

4.  Atrioventricular canal associated with trisomy 9.

Authors:  B Marino; M C Digilio; A Giannotti; B Dallapiccola
Journal:  Chest       Date:  1989-12       Impact factor: 9.410

Review 5.  Nonrandom association of atrioventricular canal and del (8p) syndrome.

Authors:  B Marino; A Reale; A Giannotti; M C Digilio; B Dallapiccola
Journal:  Am J Med Genet       Date:  1992-02-15

6.  Atrioventricular canal in Down syndrome. Prevalence of associated cardiac malformations compared with patients without Down syndrome.

Authors:  B Marino; U Vairo; A Corno; S Nava; P Guccione; R Calabrò; C Marcelletti
Journal:  Am J Dis Child       Date:  1990-10

7.  [Trisomy 18 associated with atrioventricular canal].

Authors:  M C Digilio; B Marino; A Giannotti; B Dallapiccola
Journal:  G Ital Cardiol       Date:  1991-04

8.  Endocardial cushion defect: further studies of "isolated" versus "syndromic" occurrence.

Authors:  R Carmi; J A Boughman; C Ferencz
Journal:  Am J Med Genet       Date:  1992-06-01

9.  A large, dominant pedigree of atrioventricular septal defect (AVSD): exclusion from the Down syndrome critical region on chromosome 21.

Authors:  L Wilson; A Curtis; J R Korenberg; R D Schipper; L Allan; G Chenevix-Trench; A Stephenson; J Goodship; J Burn
Journal:  Am J Hum Genet       Date:  1993-12       Impact factor: 11.025

10.  Linkage analysis of autosomal dominant atrioventricular canal defects: exclusion of chromosome 21.

Authors:  A J Cousineau; R M Lauer; M E Pierpont; T L Burns; R H Ardinger; S R Patil; V C Sheffield
Journal:  Hum Genet       Date:  1994-02       Impact factor: 4.132
View more
  3 in total

1.  Is a shorter atrioventricular septal length an intermediate phenotype in the spectrum of nonsyndromic atrioventricular septal defects?

Authors:  Sonali S Patel; Larry T Mahoney; Trudy L Burns
Journal:  J Am Soc Echocardiogr       Date:  2012-04-25       Impact factor: 5.251

Review 2.  Familial recurrence of congenital heart disease: an overview and review of the literature.

Authors:  Giulio Calcagni; M Cristina Digilio; Anna Sarkozy; Bruno Dallapiccola; Bruno Marino
Journal:  Eur J Pediatr       Date:  2006-11-08       Impact factor: 3.183

Review 3.  Genetics of atrioventricular canal defects.

Authors:  Flaminia Pugnaloni; Maria Cristina Digilio; Carolina Putotto; Enrica De Luca; Bruno Marino; Paolo Versacci
Journal:  Ital J Pediatr       Date:  2020-05-13       Impact factor: 2.638
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.