Literature DB >> 8135296

Atrioventricular canal and 8p- syndrome.

M C Digilio, A Giannotti, B Marino, B Dallapiccola.   

Abstract

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Mesh：

Year:  1993        PMID： 8135296     DOI： 10.1002/ajmg.1320470331

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  5 in total

Review 1.  Partial trisomy 1(q42-->qter): a new case with a mild phenotype.

Authors:  D Concolino; R Cinti; L Ferraro; M T Moricca; P Strisciuglio
Journal:  J Med Genet       Date:  1998-01       Impact factor: 6.318

2.  Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

Authors:  K Devriendt; G Matthijs; R Van Dael; M Gewillig; B Eyskens; H Hjalgrim; B Dolmer; J McGaughran; K Bröndum-Nielsen; P Marynen; J P Fryns; J R Vermeesch
Journal:  Am J Hum Genet       Date:  1999-04       Impact factor: 11.025

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

Authors:  M Gennarelli; G Novelli; M C Digilio; A Giannotti; B Marino; B Dallapiccola
Journal:  Hum Genet       Date:  1994-12       Impact factor: 4.132

Review 4.  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

5.  Cytogenomics Investigation of Infants with Congenital Heart Disease: Experience of a Brazilian Center.

Authors:  Marcília Sierro Grassi; Marília Montenegro; Evelin Aline Zanardo; Antonio Carlos Pastorino; Mayra Barros Dorna; Chong Kim; Marcelo Jatene; Nana Miura; Leslie Kulikowski; Magda Carneiro-Sampaio
Journal:  Arq Bras Cardiol       Date:  2022-01       Impact factor: 2.000
  5 in total

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