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Padmini Parthasarathy

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

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Maternal and Child Health Journal|June 2, 2011
Integrating the life course perspective into a local maternal and child health programCheri Pies, Padmini Parthasarathy, Samuel F Posner
Database : the Journal of Biological Databases and Curation|December 1, 2020
ncVarDB: a manually curated database for pathogenic non-coding variants and benign controlsHarry Biggs, Padmini Parthasarathy, Alexandra Gavryushkina, et al.
Maternal and Child Health Journal|June 25, 2013
Building Economic Security Today: making the health-wealth connection in Contra Costa county's maternal and child health programsPadmini Parthasarathy, Dawn E Dailey, Maria-Elena D Young, et al.
Maternal and Child Health Journal|July 16, 2024
Development and Unfolding of the Life Course Movement in the Field of Maternal and Child Health: An Oral HistoryAlessandra N Bazzano, Cheri Pies, Michael C Lu, et al.
European Journal of Human Genetics : EJHG|May 10, 2021
Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasiaEmma M Wade, Padmini Parthasarathy, Jingyi Mi, et al.
Genes|April 30, 2021
Intragenic Deletions in <i>FLNB</i> Are Part of the Mutational Spectrum Causing Spondylocarpotarsal Synostosis SyndromeKaya Fukushima, Padmini Parthasarathy, Emma M Wade, et al.
Genes|December 3, 2020
Deletion of Exon 1 in <i>AMER1</i> in Osteopathia Striata with Cranial SclerosisJingyi Mi, Padmini Parthasarathy, Benjamin J Halliday, et al.
HGG Advances|March 14, 2026
Impaired retinoic acid receptor-γ signalling underlies a heritable form of urothelial keratinising squamous metaplasiaKaya Fukushima, Nicole Avery, Jade Desjardins, et al.
Human Mutation|July 6, 2020
Biallelic loss-of-function variants in TBC1D2B cause a neurodevelopmental disorder with seizures and gingival overgrowthFrederike L Harms, Padmini Parthasarathy, Dennis Zorndt, et al.
American Journal of Human Genetics|April 28, 2021
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphismMaya Chopra, Meriel McEntagart, Jill Clayton-Smith, et al.
Pageof 1

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

Sort By:
Pageof 1
Maternal and Child Health Journal|June 2, 2011
Integrating the life course perspective into a local maternal and child health programCheri Pies, Padmini Parthasarathy, Samuel F Posner
Database : the Journal of Biological Databases and Curation|December 1, 2020
ncVarDB: a manually curated database for pathogenic non-coding variants and benign controlsHarry Biggs, Padmini Parthasarathy, Alexandra Gavryushkina, et al.
Maternal and Child Health Journal|June 25, 2013
Building Economic Security Today: making the health-wealth connection in Contra Costa county's maternal and child health programsPadmini Parthasarathy, Dawn E Dailey, Maria-Elena D Young, et al.
Maternal and Child Health Journal|July 16, 2024
Development and Unfolding of the Life Course Movement in the Field of Maternal and Child Health: An Oral HistoryAlessandra N Bazzano, Cheri Pies, Michael C Lu, et al.
European Journal of Human Genetics : EJHG|May 10, 2021
Deletion of the last two exons of FGF10 in a family with LADD syndrome and pulmonary acinar hypoplasiaEmma M Wade, Padmini Parthasarathy, Jingyi Mi, et al.
Genes|April 30, 2021
Intragenic Deletions in <i>FLNB</i> Are Part of the Mutational Spectrum Causing Spondylocarpotarsal Synostosis SyndromeKaya Fukushima, Padmini Parthasarathy, Emma M Wade, et al.
Genes|December 3, 2020
Deletion of Exon 1 in <i>AMER1</i> in Osteopathia Striata with Cranial SclerosisJingyi Mi, Padmini Parthasarathy, Benjamin J Halliday, et al.
HGG Advances|March 14, 2026
Impaired retinoic acid receptor-γ signalling underlies a heritable form of urothelial keratinising squamous metaplasiaKaya Fukushima, Nicole Avery, Jade Desjardins, et al.
Human Mutation|July 6, 2020
Biallelic loss-of-function variants in TBC1D2B cause a neurodevelopmental disorder with seizures and gingival overgrowthFrederike L Harms, Padmini Parthasarathy, Dennis Zorndt, et al.
American Journal of Human Genetics|April 28, 2021
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphismMaya Chopra, Meriel McEntagart, Jill Clayton-Smith, et al.
Pageof 1