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Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma
Article de revueAppl Clin Genet, 7 , 2014.
Cost effectiveness of newborn screening for cystic fibrosis: a simulation study
Article de revueJ Cyst Fibros, 13 (3), 2014.
Recurrent anencephaly: a case report and examination of the VANGL1 and FOXN1 genes
Article de revueFetal Pediatr Pathol, 32 (4), 2013.
Cost-effectiveness of the management of rh-negative pregnant women
Article de revueJ Obstet Gynaecol Can, 35 (8), 2013.
Molecular prenatal diagnosis of a sporadic alobar holoprosencephalic fetus: genotype-phenotype correlations
Article de revueJ Prenat Med, 6 (3), 2012.
Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria
Article de revueFetal Pediatr Pathol, 31 (5), 2012.
Myoblasts derived from normal hESCs and dystrophic hiPSCs efficiently fuse with existing muscle fibers following transplantation
Article de revueMol Ther, 20 (11), 2012.
A survey of APC mutations in Quebec
Article de revueFam Cancer, 10 (4), 2011.
Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities
Article de revueEur J Hum Genet, 19 (1), 2011.
Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation
Article de revueJ Med Genet, 48 (12), 2011.