Literature DB >> 27272050

Pre- and Postnatal Diagnosis of 5q35.1 and 8p23.1 Deletion in Congenital Heart Disease.

Mitesh Shetty1, Ambika Srikanth2, Pooja Kulshreshtha2, Jayarama Kadandale2, Sridevi Hegde3.   

Abstract

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Year:  2016        PMID： 27272050     DOI： 10.1007/s12098-016-2158-3

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


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  5 in total

1.  Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects.

Authors:  S Giglio; S L Graw; G Gimelli; B Pirola; P Varone; L Voullaire; F Lerzo; E Rossi; C Dellavecchia; M C Bonaglia; M C Digilio; A Giannotti; B Marino; R Carrozzo; J R Korenberg; C Danesino; E Sujansky; B Dallapiccola; O Zuffardi
Journal:  Circulation       Date:  2000-07-25       Impact factor: 29.690

2.  New trends in chromosomal investigation in children with cardiovascular malformations.

Authors:  Ruth Schellberg; Gesa Schwanitz; Lutz Grävinghoff; Rolf Kallenberg; Detlef Trost; Ruth Raff; Walter Wiebe
Journal:  Cardiol Young       Date:  2004-12       Impact factor: 1.093

3.  Novel NKX2-5 mutations responsible for congenital heart disease.

Authors:  J Wang; X Y Liu; Y Q Yang
Journal:  Genet Mol Res       Date:  2011-11-29

4.  GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.

Authors:  Vidu Garg; Irfan S Kathiriya; Robert Barnes; Marie K Schluterman; Isabelle N King; Cheryl A Butler; Caryn R Rothrock; Reenu S Eapen; Kayoko Hirayama-Yamada; Kunitaka Joo; Rumiko Matsuoka; Jonathan C Cohen; Deepak Srivastava
Journal:  Nature       Date:  2003-07-06       Impact factor: 49.962

5.  Delineation of a 2.2 Mb microdeletion at 5q35 associated with microcephaly and congenital heart disease.

Authors:  Marie Baekvad-Hansen; Zeynep Tümer; Alicia Delicado; Fikret Erdogan; Niels Tommerup; Lars A Larsen
Journal:  Am J Med Genet A       Date:  2006-03-01       Impact factor: 2.802
  5 in total

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