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Julie L Lauzon

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Journal of Neurosurgery. Pediatrics|October 3, 2009
Endoscopic third ventriculostomy to treat hydrocephalus associated with macrocephaly-cutis marmorata telangiectatica congenitaAlim P Mitha, Kelly J Bullivant, Julie L Lauzon, et al.
Human Reproduction (Oxford, England)|December 23, 2006
Origin and outcome of pregnancies affected by androgenetic/biparental chimerismWendy P Robinson, Julie L Lauzon, A Micheil Innes, et al.
Human Mutation|August 23, 2012
A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effectNelly Abdelfatah, Nancy Merner, Jim Houston, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 21, 2013
Novel mutations in geleophysic dysplasia type 1Prashob Porayette, Deborah Fruitman, Julie L Lauzon, et al.
Canadian Journal of Kidney Health and Disease|November 4, 2021
Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney DiseaseMark D Elliott, Leslie C James, Emily L Simms, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|November 27, 2018
Next-Generation Sequencing Using a Cardiac Gene Panel in Prenatally Diagnosed Cardiac AnomaliesRyan E Lamont, Yanwei Xi, Claire Popko, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2022
De novo variants in the PABP domain of PABPC1 lead to developmental delayMeret Wegler, Xiangbin Jia, Marielle Alders, et al.
Prenatal Diagnosis|April 22, 2009
Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardiaAngela E Lin, Barbara O'Brien, Laurie A Demmer, et al.
Neuron|April 4, 2020
A Cluster of Autism-Associated Variants on X-Linked NLGN4X Functionally Resemble NLGN4YThien A Nguyen, Kunwei Wu, Saurabh Pandey, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patientsRobert L Conway, Barry D Pressman, William B Dobyns, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Journal of Neurosurgery. Pediatrics|October 3, 2009
Endoscopic third ventriculostomy to treat hydrocephalus associated with macrocephaly-cutis marmorata telangiectatica congenitaAlim P Mitha, Kelly J Bullivant, Julie L Lauzon, et al.
Human Reproduction (Oxford, England)|December 23, 2006
Origin and outcome of pregnancies affected by androgenetic/biparental chimerismWendy P Robinson, Julie L Lauzon, A Micheil Innes, et al.
Human Mutation|August 23, 2012
A novel deletion in SMPX causes a rare form of X-linked progressive hearing loss in two families due to a founder effectNelly Abdelfatah, Nancy Merner, Jim Houston, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|November 21, 2013
Novel mutations in geleophysic dysplasia type 1Prashob Porayette, Deborah Fruitman, Julie L Lauzon, et al.
Canadian Journal of Kidney Health and Disease|November 4, 2021
Mainstreaming Genetic Testing for Adult Patients With Autosomal Dominant Polycystic Kidney DiseaseMark D Elliott, Leslie C James, Emily L Simms, et al.
Journal of Obstetrics and Gynaecology Canada : JOGC = Journal D'Obstetrique Et Gynecologie Du Canada : JOGC|November 27, 2018
Next-Generation Sequencing Using a Cardiac Gene Panel in Prenatally Diagnosed Cardiac AnomaliesRyan E Lamont, Yanwei Xi, Claire Popko, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2022
De novo variants in the PABP domain of PABPC1 lead to developmental delayMeret Wegler, Xiangbin Jia, Marielle Alders, et al.
Prenatal Diagnosis|April 22, 2009
Prenatal features of Costello syndrome: ultrasonographic findings and atrial tachycardiaAngela E Lin, Barbara O'Brien, Laurie A Demmer, et al.
Neuron|April 4, 2020
A Cluster of Autism-Associated Variants on X-Linked NLGN4X Functionally Resemble NLGN4YThien A Nguyen, Kunwei Wu, Saurabh Pandey, et al.
American Journal of Medical Genetics. Part A|November 15, 2007
Neuroimaging findings in macrocephaly-capillary malformation: a longitudinal study of 17 patientsRobert L Conway, Barry D Pressman, William B Dobyns, et al.
Pageof 2