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David J Amor

Showing results (71-80 of 275) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2026
Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infantsDavid E Godler, Ling Ling, Dinusha Gamage, et al.
Developmental Medicine and Child Neurology|November 18, 2020
First-trimester maternal serum biomarkers and the risk of cerebral palsyMonique Peris, Susan M Reid, Stephen Dobie, et al.
Prenatal Diagnosis|July 16, 2021
Second trimester maternal serum biomarkers and the risk of cerebral palsyMonique Peris, Susan M Reid, Stephen Dobie, et al.
Reproductive Health|February 11, 2018
Attitudes of sperm, egg and embryo donors and recipients towards genetic information and screening of donorsDavid J Amor, Annabelle Kerr, Nandini Somanathan, et al.
American Journal of Medical Genetics. Part A|October 27, 2020
Lymphedema distichiasis syndrome may be caused by FOXC2 promoter-enhancer dissociation and disruption of a topological associated domainMathew Wallis, Rachel Pope-Couston, Julia Mansour, et al.
Plos Genetics|December 16, 2016
Loss of RMI2 Increases Genome Instability and Causes a Bloom-Like SyndromeDamien F Hudson, David J Amor, Amber Boys, et al.
Developmental Medicine and Child Neurology|July 7, 2023
Causation in cerebral palsy: Parental beliefs and associated emotionsRenée Smyth, Susan M Reid, Kate Paton, et al.
Molecular Psychiatry|February 17, 2024
Genetic architecture of childhood speech disorder: a reviewAngela T Morgan, David J Amor, Miya D St John, et al.
European Journal of Human Genetics : EJHG|December 9, 2024
Parental attitudes and experiences in pursuing genetic testing for their child's motor speech disorderChristy Atkinson, Yong Quan Lee, Mariana L Lauretta, et al.
BMC Pediatrics|October 11, 2021
Study protocol: childhood outcomes of fetal genomic variants: the PrenatAL Microarray (PALM) cohort studyLisa Hui, Cecilia Pynaker, Joanne Kennedy, et al.
Pageof 28

Showing results (71-80 of 275) with videos related to

Sort By:
Pageof 28
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 8, 2026
Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infantsDavid E Godler, Ling Ling, Dinusha Gamage, et al.
Developmental Medicine and Child Neurology|November 18, 2020
First-trimester maternal serum biomarkers and the risk of cerebral palsyMonique Peris, Susan M Reid, Stephen Dobie, et al.
Prenatal Diagnosis|July 16, 2021
Second trimester maternal serum biomarkers and the risk of cerebral palsyMonique Peris, Susan M Reid, Stephen Dobie, et al.
Reproductive Health|February 11, 2018
Attitudes of sperm, egg and embryo donors and recipients towards genetic information and screening of donorsDavid J Amor, Annabelle Kerr, Nandini Somanathan, et al.
American Journal of Medical Genetics. Part A|October 27, 2020
Lymphedema distichiasis syndrome may be caused by FOXC2 promoter-enhancer dissociation and disruption of a topological associated domainMathew Wallis, Rachel Pope-Couston, Julia Mansour, et al.
Plos Genetics|December 16, 2016
Loss of RMI2 Increases Genome Instability and Causes a Bloom-Like SyndromeDamien F Hudson, David J Amor, Amber Boys, et al.
Developmental Medicine and Child Neurology|July 7, 2023
Causation in cerebral palsy: Parental beliefs and associated emotionsRenée Smyth, Susan M Reid, Kate Paton, et al.
Molecular Psychiatry|February 17, 2024
Genetic architecture of childhood speech disorder: a reviewAngela T Morgan, David J Amor, Miya D St John, et al.
European Journal of Human Genetics : EJHG|December 9, 2024
Parental attitudes and experiences in pursuing genetic testing for their child's motor speech disorderChristy Atkinson, Yong Quan Lee, Mariana L Lauretta, et al.
BMC Pediatrics|October 11, 2021
Study protocol: childhood outcomes of fetal genomic variants: the PrenatAL Microarray (PALM) cohort studyLisa Hui, Cecilia Pynaker, Joanne Kennedy, et al.
Pageof 28