Literature DB >> 10334453

Guidelines for 22q11 deletion screening of patients with conotruncal defects.

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

Abstract

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Year:  1999        PMID： 10334453     DOI： 10.1016/s0735-1097(99)00084-4

Source DB:  PubMed          Journal:  J Am Coll Cardiol        ISSN： 0735-1097            Impact factor:   24.094


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  5 in total

1.  A rare association of interrupted aortic arch type C and microdeletion 22q11.2.

Authors:  Goran Cuturilo; Danijela Drakulic; Milena Stevanovic; Ida Jovanovic; Milan Djukic; Slobodanka Miletic-Grkovic; Marina Atanaskovic-Markovic
Journal:  Eur J Pediatr       Date:  2007-11-27       Impact factor: 3.183

2.  Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India.

Authors:  Ashutosh Halder; Manish Jain; Isha Chaudhary; Madhulika Kabra
Journal:  BMC Med Genet       Date:  2010-06-23       Impact factor: 2.103

3.  Extracardiac features predicting 22q11.2 deletion syndrome in adult congenital heart disease.

Authors:  Wai Lun Alan Fung; Eva W C Chow; Gary D Webb; Michael A Gatzoulis; Anne S Bassett
Journal:  Int J Cardiol       Date:  2008-01-11       Impact factor: 4.164

4.  The fate of children with microdeletion 22q11.2 syndrome and congenital heart defect: clinical course and cardiac outcome.

Authors:  A Kyburz; U Bauersfeld; A Schinzel; M Riegel; M Hug; M Tomaske; E R Valsangiacomo Büchel
Journal:  Pediatr Cardiol       Date:  2007-09-29       Impact factor: 1.655

5.  Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome).

Authors:  Mc Digilio; B Marino; R Capolino; B Dallapiccola
Journal:  Images Paediatr Cardiol       Date:  2005-04
  5 in total

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