scholarly journals Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients

2004 ◽  
Vol 41 (4) ◽  
pp. e40-e40 ◽  
Author(s):  
A Rauch
Keyword(s):  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
22Q11.2 Deletion ◽  
Tbx1 Gene

scholarly journals Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

2016 ◽  
Vol 135 (3) ◽  
pp. 273-285 ◽  
Author(s):  
Elisabeth E. Mlynarski ◽  
◽  
Michael Xie ◽  
Deanne Taylor ◽  
Molly B. Sheridan ◽  
...  
Keyword(s):  
Congenital Heart Defects ◽  
Copy Number ◽  
Congenital Heart ◽  
Heart Defects ◽  
Copy Number Variants ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
22Q11.2 Deletion

Congenital Heart Defects and Measures of Fetal Growth in Newborns with Down Syndrome or 22q11.2 Deletion Syndrome

2016 ◽  
Vol 175 ◽  
pp. 116-122.e4 ◽  
Author(s):  
Niels B. Matthiesen ◽  
Peter Agergaard ◽  
Tine B. Henriksen ◽  
Cathrine C. Bach ◽  
J. William Gaynor ◽  
...  
Keyword(s):  
Down Syndrome ◽  
Fetal Growth ◽  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
22Q11.2 Deletion

scholarly journals 22q11.2 deletion syndrome and complex congenital heart defects

2011 ◽  
Vol 57 (1) ◽  
pp. 62-65
Author(s):  
Rafael Fabiano Machado Rosa ◽  
Patrícia Trevisan ◽  
Dayane Bohn Koshiyama ◽  
Carlo Benatti Pilla ◽  
Paulo Ricardo Gazzola Zen ◽  
...  
Keyword(s):  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
22Q11.2 Deletion

The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon

Global Heart ◽  
2017 ◽  
Vol 12 (2) ◽  
pp. 115 ◽  
Author(s):  
Ambroise Wonkam ◽  
Ricardo Toko ◽  
David Chelo ◽  
Cedrik Tekendo-Ngongang ◽  
Samuel Kingue ◽  
...  
Keyword(s):  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
Microdeletion Syndrome ◽  
22Q11.2 Deletion

scholarly journals 22q11.2 deletion syndrome and complex congenital heart defects

2011 ◽  
Vol 57 (1) ◽  
pp. 62-65 ◽  
Author(s):  
Rafael Fabiano Machado Rosa ◽  
Patrícia Trevisan ◽  
Dayane Bohn Koshiyama ◽  
Carlo Benatti Pilla ◽  
Paulo Ricardo Gazzola Zen ◽  
...  
Keyword(s):  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
22Q11.2 Deletion Syndrome ◽  
Deletion Syndrome ◽  
22Q11.2 Deletion

Congenital heart defects in a novel recurrent 22q11.2 deletion harboring the genes CRKL and MAPK1

2012 ◽  
Vol 158A (3) ◽  
pp. 574-580 ◽  
Author(s):  
Jeroen Breckpot ◽  
Bernard Thienpont ◽  
Marijke Bauters ◽  
Leon-Charles Tranchevent ◽  
Marc Gewillig ◽  
...  
Keyword(s):  
Congenital Heart Defects ◽  
Congenital Heart ◽  
Heart Defects ◽  
22Q11.2 Deletion
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