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Shereen Tadros

Showing results (1-10 of 12) with videos related to

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Current Genetic Medicine Reports|November 30, 2020
From Beyond the Grave: Use of Medical Information from the Deceased to Guide Care of Living RelativesShereen Tadros, Helena Carley, Anneke Lucassen
Archives of Disease in Childhood. Education and Practice Edition|June 1, 2013
What is array CGH?Shereen Tadros, Deborah Morrogh, Richard H Scott
BMJ Case Reports|September 3, 2011
Liver abscess within the first week of life in a very low birthweight infantKhalid Mannan, Shereen Tadros, Kamini Patel, et al.
Clinical Dysmorphology|September 8, 2020
When Rothmund-Thomson syndrome is not: two new cases of Clericuzio-type poikiloderma with neutropeniaShereen Tadros, Karina Forde, Samira Syed, et al.
Clinical Dysmorphology|August 31, 2016
Metaphyseal dysplasia, Spahr type; missense MMP13 mutations in two Iraqi siblingsShereen Tadros, Richard H Scott, Alistair D Calder, et al.
Future Healthcare Journal|May 20, 2024
Preparing tomorrow's doctors for the genomics era: A nationwide survey of UK medical studentsLydia Seed, Anna Scott, Michelle Peter, et al.
BMJ Open|September 24, 2024
Perceptions of genomic newborn screening: a cross-sectional survey conducted with UK medical studentsLydia Seed, Anna Scott, Amanda Pichini, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Inherited 2q23.1 microdeletions involving the <i>MBD5</i> locusShereen Tadros, Rubin Wang, Jonathan J Waters, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disordersAlistair T Pagnamenta, Yoshiko Murakami, John M Taylor, et al.
Medrxiv : the Preprint Server for Health Sciences|February 26, 2024
Biallelic variation in the choline and ethanolamine transporter <i>FLVCR1</i> underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disordersDaniel G Calame, Jovi Huixin Wong, Puravi Panda, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Current Genetic Medicine Reports|November 30, 2020
From Beyond the Grave: Use of Medical Information from the Deceased to Guide Care of Living RelativesShereen Tadros, Helena Carley, Anneke Lucassen
Archives of Disease in Childhood. Education and Practice Edition|June 1, 2013
What is array CGH?Shereen Tadros, Deborah Morrogh, Richard H Scott
BMJ Case Reports|September 3, 2011
Liver abscess within the first week of life in a very low birthweight infantKhalid Mannan, Shereen Tadros, Kamini Patel, et al.
Clinical Dysmorphology|September 8, 2020
When Rothmund-Thomson syndrome is not: two new cases of Clericuzio-type poikiloderma with neutropeniaShereen Tadros, Karina Forde, Samira Syed, et al.
Clinical Dysmorphology|August 31, 2016
Metaphyseal dysplasia, Spahr type; missense MMP13 mutations in two Iraqi siblingsShereen Tadros, Richard H Scott, Alistair D Calder, et al.
Future Healthcare Journal|May 20, 2024
Preparing tomorrow's doctors for the genomics era: A nationwide survey of UK medical studentsLydia Seed, Anna Scott, Michelle Peter, et al.
BMJ Open|September 24, 2024
Perceptions of genomic newborn screening: a cross-sectional survey conducted with UK medical studentsLydia Seed, Anna Scott, Amanda Pichini, et al.
Molecular Genetics & Genomic Medicine|September 26, 2017
Inherited 2q23.1 microdeletions involving the <i>MBD5</i> locusShereen Tadros, Rubin Wang, Jonathan J Waters, et al.
European Journal of Human Genetics : EJHG|March 23, 2017
Analysis of exome data for 4293 trios suggests GPI-anchor biogenesis defects are a rare cause of developmental disordersAlistair T Pagnamenta, Yoshiko Murakami, John M Taylor, et al.
Medrxiv : the Preprint Server for Health Sciences|February 26, 2024
Biallelic variation in the choline and ethanolamine transporter <i>FLVCR1</i> underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disordersDaniel G Calame, Jovi Huixin Wong, Puravi Panda, et al.
Pageof 2