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22q11.2 deletion mosaicism in patients with conotruncal heart defectsLI JIANRONG; LIU YINGLONG; LV XIAODONG et al.Birth defects research. Clinical and molecular teratology. 2006, Vol 76, Num 4, pp 262-265, issn 1542-0752, 4 p.Article

Tetralogy of Fallot Associated With Pulmonary Atresia and Major Aortopulmonary Collateral Arteries in a Patient With Interstitial Deletion of 16q21-q22.1YAMAMOTO, Toshiyuki; DOWA, Yuri; UEDA, Hideaki et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 12, pp 1575-1580, issn 1552-4825, 6 p.Article

Chromosome 22qll.2 microdeletion in children with conotruncal heart defects : frequency, associated cardiovascular anomalies, and outcome following cardiac surgeryZIOLKOWSKA, Lidia; KAWALEC, Wanda; TURSKA-KMIEC, Anna et al.European journal of pediatrics. 2008, Vol 167, Num 10, pp 1135-1140, issn 0340-6199, 6 p.Article

Congenital Heart Defects in Patients With Oculo-Auriculo-Vertebral Spectrum (Goldenhar Syndrome)CRISTINA DIGILIO, M; CALZOLARI, Flaminia; CAPOLINO, Rossella et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 14, pp 1815-1819, issn 1552-4825, 5 p.Article

CARDIAC DEFECTS AND RESULTS OF CARDIAC SURGERY IN 22Q11.2 DELETION SYNDROMECAROTTI, Adriano; CRISTINA DIGILIO, Maria; PIACENTINI, Gerardo et al.Developmental disabilities research reviews. 2008, Vol 14, Num 1, pp 35-42, 8 p.Article

22q11.2 Deletion Syndrome in Patients Admitted to a Cardiac Pediatric Intensive Care Unit in BrazilROSA, Rafael F. M; PILLA, Carlo B; PASKULIN, Giorgio A et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 13, pp 1655-1661, issn 1552-4825, 7 p.Article

Prenatally diagnosed fetal lung lesions with associated conotruncal heart defects : Is there a genetic association?HIISLER, Margaret R; WILSON, R. Douglas; RYCHIK, Jack et al.Prenatal diagnosis. 2007, Vol 27, Num 12, pp 1123-1128, issn 0197-3851, 6 p.Article

Cardiovascular malformations in fryns syndrome : Is there a pathogenic role for neural crest cells?LIN, Angela E; POBER, Barbara R; MULLEN, Mary P et al.American journal of medical genetics. 2005, Vol 139A, Num 3, pp 186-193, issn 0148-7299, 8 p.Article

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