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Pregnancy Outcomes After Assisted Reproductive Technology

Journal of obstetrics and gynaecology Canada, 2006-03, Vol.28 (3), p.220-233

2006

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RETIRED: Pregnancy Outcomes After Assisted Reproductive Technology

Journal of obstetrics and gynaecology Canada, 2006-03, Vol.28 (3), p.220-233

2006

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Issues de grossesse à la suite du recours aux techniques de procréation assistée

Journal of obstetrics and gynaecology Canada, 2006-03, Vol.28 (3), p.234-250

2006

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Archivée: Issues de grossesse à la suite du recours aux techniques de procréation assistée

Journal of obstetrics and gynaecology Canada, 2006-03, Vol.28 (3), p.234-250

2006

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Efficacy and safety of one anastomosis gastric bypass versus Roux-en-Y gastric bypass for obesity (YOMEGA): a multicentre, randomised, open-label, non-inferiority trial

The Lancet (British edition), 2019-03, Vol.393 (10178), p.1299-1309

2019

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Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

BMC genomics, 2017-05, Vol.18 (1), p.403-403, Article 403

2017

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Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: Need for greater adherence to published guidelines

Prenatal diagnosis, 2022-11, Vol.42 (12), p.1514-1524

2022

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Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes

European journal of human genetics : EJHG, 2014-06, Vol.22 (6), p.792-800

2014

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Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women

Cochrane database of systematic reviews, 2017-11, Vol.11 (11), p.CD011767

2017

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The practice of genomic medicine: A delineation of the process and its governing principles

Frontiers in medicine, 2023-01, Vol.9, p.1071348-1071348

2023

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Tif1γ Suppresses Murine Pancreatic Tumoral Transformation by a Smad4-Independent Pathway

The American journal of pathology, 2012-06, Vol.180 (6), p.2214-2221

2012

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Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues

Application of clinical genetics, 2016-01, Vol.9 (Issue 1), p.15-26

2016

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Absence of CD47 in vivo influences thymic dendritic cell subset proportions but not negative selection of thymocytes

International immunology, 2009-02, Vol.21 (2), p.167-177

2009

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Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children

Journal of medical genetics, 2007-09, Vol.44 (9), p.556-561

2007

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

Application of clinical genetics, 2014-01, Vol.7 (default), p.127-131

2014

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Structural and functional analysis of a new desmin variant causing desmin-related myopathy

Human mutation, 2001-11, Vol.18 (5), p.388-396

2001

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The spectrum of mutations in UBE3A causing Angelman syndrome

Human molecular genetics, 1999, Vol.8 (1), p.129-135

1999

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Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes

Genomics (San Diego, Calif.), 2006-06, Vol.87 (6), p.704-710

2006

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A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation

The Journal of clinical investigation, 2000-08, Vol.106 (3), p.431-438

2000

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Nondisjunction of chromosome 15 : origin and recombination

American journal of human genetics, 1993-09, Vol.53 (3), p.740-751

1993

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MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS

Prenatal diagnosis, 1997-05, Vol.17 (5), p.443-450

1997

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Evidence for multi-site closure of the neural tube in humans

American journal of medical genetics, 1993-10, Vol.47 (5), p.723-743

1993

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Iron chelators: in vitro inhibitory effect on the liver stage of rodent and human malaria

The American journal of tropical medicine and hygiene, 1988-09, Vol.39 (3), p.236

1988

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Plasmodium ovale: In vitro development of hepatic stages

Experimental parasitology, 1987-12, Vol.64 (3), p.393-400

1987

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Interstitial 7q deletion [46,XX,del(7)(pter → q21.1::q22 → qter)] and the location of genes for β-glucuronidase and cystic fibrosis

American journal of medical genetics, 1988-11, Vol.31 (3), p.655-661

1988

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Pregnancy Outcomes After Assisted Reproductive Technology

RETIRED: Pregnancy Outcomes After Assisted Reproductive Technology

Issues de grossesse à la suite du recours aux techniques de procréation assistée

Archivée: Issues de grossesse à la suite du recours aux techniques de procréation assistée

Efficacy and safety of one anastomosis gastric bypass versus Roux-en-Y gastric bypass for obesity (YOMEGA): a multicentre, randomised, open-label, non-inferiority trial

Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

Impact of variation in practice in the prenatal reporting of variants of uncertain significance by commercial laboratories: Need for greater adherence to published guidelines

Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes

Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women

The practice of genomic medicine: A delineation of the process and its governing principles

Tif1γ Suppresses Murine Pancreatic Tumoral Transformation by a Smad4-Independent Pathway

Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues

Absence of CD47 in vivo influences thymic dendritic cell subset proportions but not negative selection of thymocytes

Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three children

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

Structural and functional analysis of a new desmin variant causing desmin-related myopathy

The spectrum of mutations in UBE3A causing Angelman syndrome

Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes

A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation

Nondisjunction of chromosome 15 : origin and recombination

MATERNAL UNIPARENTAL DISOMY OF CHROMOSOME 2 AND CONFINED PLACENTAL MOSAICISM FOR TRISOMY 2 IN A FETUS WITH INTRAUTERINE GROWTH RESTRICTION, HYPOSPADIAS, AND OLIGOHYDRAMNIOS

Evidence for multi-site closure of the neural tube in humans

Iron chelators: in vitro inhibitory effect on the liver stage of rodent and human malaria

Plasmodium ovale: In vitro development of hepatic stages

Interstitial 7q deletion [46,XX,del(7)(pter → q21.1::q22 → qter)] and the location of genes for β-glucuronidase and cystic fibrosis

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