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Fetal arthrogryposis multiplex congenita/fetal akinesia deformation sequence (FADS)—Aetiology, diagnosis, and management

Prenatal diagnosis, 2019-08, Vol.39 (9), p.720-731

2019

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Technical Update No. 436: Classification of Cesarean Deliveries in Canada: The Modified Robson Criteria

Journal of obstetrics and gynaecology Canada, 2023-05, Vol.45 (5), p.338-341.e1

2023

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Mise à jour technique N° 436 : Classification des césariennes au Canada : Critères de Robson modifiés

Journal of obstetrics and gynaecology Canada, 2023-05, Vol.45 (5), p.342-345.e1

2023

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Guideline No. 452: Diagnosis and Management of Intrahepatic Cholestasis of Pregnancy

Journal of obstetrics and gynaecology Canada, 2024-08, Vol.46 (8), p.102618, Article 102618

2024

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Directive clinique no 452 : Diagnostic et prise en charge de la cholestase intrahépatique de la grossesse

Journal of obstetrics and gynaecology Canada, 2024-08, Vol.46 (8), p.102619, Article 102619

2024

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Critical period of nonpromoter DNA methylation acquisition during prenatal male germ cell development

PloS one, 2011-09, Vol.6 (9), p.e24156-e24156

2011

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Guideline No. 441: Antenatal Fetal Health Surveillance

Journal of obstetrics and gynaecology Canada, 2023-09, Vol.45 (9), p.665-677.e3

2023

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Myasthenia gravis in pregnancy: Systematic review and case series

Obstetric medicine, 2022-06, Vol.15 (2), p.108-117

2022

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Modulation of imprinted gene expression following superovulation

Molecular and cellular endocrinology, 2014-05, Vol.388 (1-2), p.51-57

2014

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Surgical Management Algorithm for Caesarean Scar Pregnancy

Journal of obstetrics and gynaecology Canada, 2017-08, Vol.39 (8), p.619-626

2017

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Comparison of cesarean versus vaginal delivery of extremely preterm gestations in breech presentation: retrospective cohort study

The journal of maternal-fetal & neonatal medicine, 2019-04, Vol.32 (7), p.1142-1147

2019

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Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency

Clinical genetics, 2020-12, Vol.98 (6), p.613-619

2020

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Stability of DNA Methylation Patterns in Mouse Spermatogonia Under Conditions of MTHFR Deficiency and Methionine Supplementation

Biology of reproduction, 2013-11, Vol.89 (5), p.125-125

2013

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Stability of DNA Methylation Patterns in Mouse Spermatogonia Under Conditions of MTHFR Deficiency and Methionine Supplementation1

Biology of reproduction, 2013-11, Vol.89 (5)

2013

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Mise à jour technique N° 436 : Classification des césariennes au Canada : Critères de Robson modifiés

Journal of obstetrics and gynaecology Canada, 2023-05, Vol.45 (5), p.342-345.e1

2023

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Directive clinique no 452 : Diagnostic et prise en charge de la cholestase intrahépatique de la grossesse

Journal of obstetrics and gynaecology Canada, 2024-08, Vol.46 (8), Article 102619

2024

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Directive clinique n o 452 : Diagnostic et prise en charge de la cholestase intrahépatique de la grossesse

Journal of obstetrics and gynaecology Canada, 2024-08, Vol.46 (8), p.102619

2024

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Prenatal diagnosis, 2019-08, Vol.39 (9)

2019

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Directive clinique no 441 : Surveillance prénatale du bien-être fœtal

Journal of obstetrics and gynaecology Canada, 2023-09, Vol.45 (9), p.678-693.e3

2023

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Directive clinique no 441 : Surveillance prénatale du bien-être fœtal

Journal of obstetrics and gynaecology Canada, 2023-09, Vol.45 (9), p.678-693.e3

2023

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Epigenetic modification of the gene for the vitamin B12 chaperone MMACHC can result in increased tumorigenicity and methionine dependence

Molecular genetics and metabolism, 2009-04, Vol.96 (4), p.261-267

2009

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The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?

American journal of medical genetics. Part A, 2020-09, Vol.182 (9), p.2058-2067

2020

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DNA Methylation Defects in Prenatal and Postnatal Germ Cells of Dnmt3L Haploinsufficient Male Mice

Biology of reproduction, 2012-08, Vol.87 (Suppl_1), p.271-271

2012

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344: Mode of delivery of infants in breech presentation at borderline viability

American journal of obstetrics and gynecology, 2015, Vol.212 (1), p.S182-S182

2015

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Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype

Human mutation, 2006-01, Vol.27 (1), p.31-43

2006

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Fetal arthrogryposis multiplex congenita/fetal akinesia deformation sequence (FADS)—Aetiology, diagnosis, and management

Technical Update No. 436: Classification of Cesarean Deliveries in Canada: The Modified Robson Criteria

Mise à jour technique N° 436 : Classification des césariennes au Canada : Critères de Robson modifiés

Guideline No. 452: Diagnosis and Management of Intrahepatic Cholestasis of Pregnancy

Directive clinique no 452 : Diagnostic et prise en charge de la cholestase intrahépatique de la grossesse

Critical period of nonpromoter DNA methylation acquisition during prenatal male germ cell development

Guideline No. 441: Antenatal Fetal Health Surveillance

Myasthenia gravis in pregnancy: Systematic review and case series

Modulation of imprinted gene expression following superovulation

Surgical Management Algorithm for Caesarean Scar Pregnancy

Comparison of cesarean versus vaginal delivery of extremely preterm gestations in breech presentation: retrospective cohort study

Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency

Stability of DNA Methylation Patterns in Mouse Spermatogonia Under Conditions of MTHFR Deficiency and Methionine Supplementation

Stability of DNA Methylation Patterns in Mouse Spermatogonia Under Conditions of MTHFR Deficiency and Methionine Supplementation1

Mise à jour technique N° 436 : Classification des césariennes au Canada : Critères de Robson modifiés

Directive clinique no 452 : Diagnostic et prise en charge de la cholestase intrahépatique de la grossesse

Directive clinique n o 452 : Diagnostic et prise en charge de la cholestase intrahépatique de la grossesse

Cover Image

Directive clinique no 441 : Surveillance prénatale du bien-être fœtal

Directive clinique no 441 : Surveillance prénatale du bien-être fœtal

Epigenetic modification of the gene for the vitamin B12 chaperone MMACHC can result in increased tumorigenicity and methionine dependence

The variability of SMARCA4‐related Coffin–Siris syndrome: Do nonsense candidate variants add to milder phenotypes?

DNA Methylation Defects in Prenatal and Postnatal Germ Cells of Dnmt3L Haploinsufficient Male Mice

344: Mode of delivery of infants in breech presentation at borderline viability

Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype

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