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32 enregistrements « 2 de 4 »

Gekas J, Langlois S, Ravitsky V, Audibert F, van den Berg DG, Haidar H, Rousseau F

Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma

Article de revue

Appl Clin Genet, 7 , 2014.

Résumé | Liens:

Nshimyumukiza L, Bois A, Daigneault P, Lands L, Laberge AM, Fournier D, Duplantie J, Giguere Y, Gekas J, Gagne C, Rousseau F, Reinharz D

Cost effectiveness of newborn screening for cystic fibrosis: a simulation study

Article de revue

J Cyst Fibros, 13 (3), 2014.

Résumé | Liens:

Sergi C, Gekas J, Kamnasaran D

Recurrent anencephaly: a case report and examination of the VANGL1 and FOXN1 genes

Article de revue

Fetal Pediatr Pathol, 32 (4), 2013.

Résumé | Liens:

Duplantie J, Gonzales OM, Bois A, Nshimyumukiza L, Gekas J, Bujold E, Morin V, Vallee M, Giguere Y, Gagne C, Rousseau F, Reinharz D

Cost-effectiveness of the management of rh-negative pregnant women

Article de revue

J Obstet Gynaecol Can, 35 (8), 2013.

Résumé | Liens:

Gekas J, Sergi C, Kamnasaran D

Molecular prenatal diagnosis of a sporadic alobar holoprosencephalic fetus: genotype-phenotype correlations

Article de revue

J Prenat Med, 6 (3), 2012.

Résumé | Liens:

Sergi C, Gekas J, Kamnasaran D

Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria

Article de revue

Fetal Pediatr Pathol, 31 (5), 2012.

Résumé | Liens:

Goudenege S, Lebel C, Huot NB, Dufour C, Fujii I, Gekas J, Rousseau J, Tremblay JP

Myoblasts derived from normal hESCs and dystrophic hiPSCs efficiently fuse with existing muscle fibers following transplantation

Article de revue

Mol Ther, 20 (11), 2012.

Résumé | Liens:

Jarry J, Brunet JS, Laframboise R, Drouin R, Latreille J, Richard C, Gekas J, Maranda B, Monczak Y, Wong N, Pouchet C, Zaor S, Kasprzak L, Palma L, Wu MK, Tischkowitz M, Foulkes WD, Chong G

A survey of APC mutations in Quebec

Article de revue

Fam Cancer, 10 (4), 2011.

Résumé | Liens:

Gekas J, van den Berg DG, Durand A, Vallee M, Wildschut HI, Bujold E, Forest JC, Rousseau F, Reinharz D

Rapid testing versus karyotyping in Down's syndrome screening: cost-effectiveness and detection of clinically significant chromosome abnormalities

Article de revue

Eur J Hum Genet, 19 (1), 2011.

Résumé | Liens:

Gekas J, Vallee M, Castonguay L, Laframboise R, Maranda B, Piedboeuf B, Rousseau F

Clinical validity of karyotyping for the diagnosis of chromosomal imbalance following array comparative genomic hybridisation

Article de revue

J Med Genet, 48 (12), 2011.

Résumé | Liens:

32 enregistrements « 2 de 4 »
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