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David Chitayat

Showing results (41-50 of 352) with videos related to

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Human Mutation|January 16, 2007
MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identifiedRosa Ferrentino, Maria Teresa Bassi, David Chitayat, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|November 16, 2011
Prenatal screening for fetal aneuploidyDavid Chitayat, Sylvie Langlois, Alain Gagnon, et al.
Prenatal Diagnosis|September 3, 2024
Agenesis of Corpus Callosum, Malformations of Cortical Development, Duodenal Atresia and Fetal Growth Restriction: Prenatal Markers for Zhu-Tokita-Takenouchi-Kim SyndromeLaurence Sophie Carmant, Elka Miller, Karen Chong, et al.
Fetal Diagnosis and Therapy|August 17, 2006
First trimester ultrasound diagnosis of lethal multiple pterygium syndromeMunire Gundogan, Katherine Fong, Sarah Keating, et al.
Lancet (London, England)|August 22, 2006
Pharmacogenetics of morphine poisoning in a breastfed neonate of a codeine-prescribed motherGideon Koren, James Cairns, David Chitayat, et al.
Pediatric Neurology|October 22, 2013
Eye and brain abnormalities in congenital muscular dystrophies caused by fukutin-related protein gene (FKRP) mutationsMaina Kava, David Chitayat, Susan Blaser, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 5, 2006
Perinatal and neurodevelopmental outcome with isolated fetal ventriculomegaly: a systematic reviewMatthew D Laskin, John Kingdom, Ants Toi, et al.
Cardiology in the Young|May 8, 2008
Prenatal diagnosis of topsy-turvy heartEdgar Jaeggi, David Chitayat, Fraser Golding, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
XY sex reversal, pontocerebellar hypoplasia and intellectual disability: confirmation of a new syndromeKomudi Siriwardena, Almundher Al-Maawali, Andrea Guerin, et al.
NDT Plus|May 8, 2015
A novel disease-causing mutation in AVPR2: Q96HMathieu Lemaire, David Chitayat, Denis F Geary, et al.
Pageof 36

Showing results (41-50 of 352) with videos related to

Sort By:
Pageof 36
Human Mutation|January 16, 2007
MID1 mutation screening in a large cohort of Opitz G/BBB syndrome patients: twenty-nine novel mutations identifiedRosa Ferrentino, Maria Teresa Bassi, David Chitayat, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|November 16, 2011
Prenatal screening for fetal aneuploidyDavid Chitayat, Sylvie Langlois, Alain Gagnon, et al.
Prenatal Diagnosis|September 3, 2024
Agenesis of Corpus Callosum, Malformations of Cortical Development, Duodenal Atresia and Fetal Growth Restriction: Prenatal Markers for Zhu-Tokita-Takenouchi-Kim SyndromeLaurence Sophie Carmant, Elka Miller, Karen Chong, et al.
Fetal Diagnosis and Therapy|August 17, 2006
First trimester ultrasound diagnosis of lethal multiple pterygium syndromeMunire Gundogan, Katherine Fong, Sarah Keating, et al.
Lancet (London, England)|August 22, 2006
Pharmacogenetics of morphine poisoning in a breastfed neonate of a codeine-prescribed motherGideon Koren, James Cairns, David Chitayat, et al.
Pediatric Neurology|October 22, 2013
Eye and brain abnormalities in congenital muscular dystrophies caused by fukutin-related protein gene (FKRP) mutationsMaina Kava, David Chitayat, Susan Blaser, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|January 5, 2006
Perinatal and neurodevelopmental outcome with isolated fetal ventriculomegaly: a systematic reviewMatthew D Laskin, John Kingdom, Ants Toi, et al.
Cardiology in the Young|May 8, 2008
Prenatal diagnosis of topsy-turvy heartEdgar Jaeggi, David Chitayat, Fraser Golding, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
XY sex reversal, pontocerebellar hypoplasia and intellectual disability: confirmation of a new syndromeKomudi Siriwardena, Almundher Al-Maawali, Andrea Guerin, et al.
NDT Plus|May 8, 2015
A novel disease-causing mutation in AVPR2: Q96HMathieu Lemaire, David Chitayat, Denis F Geary, et al.
Pageof 36