Jean GekasM.D.

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

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

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

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

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

J Prenat Med, 6 (3), 2012.

Résumé | Liens:

Sergi C, Gekas J, Kamnasaran D

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

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

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

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

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

J Med Genet, 48 (12), 2011.

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