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Nature Genetics
|
October 27, 2014
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy
Carol-Anne Martin, Ilyas Ahmad, Anna Klingseisen, et al.
Human Mutation
|
June 18, 2019
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita
Suzanna G M Frints, Friederike Hennig, Roberto Colombo, et al.
European Heart Journal
|
May 28, 2024
Atherosclerosis in ancient mummified humans: the global HORUS study
Randall C Thompson, M Linda Sutherland, Adel H Allam, et al.
Human Molecular Genetics
|
September 10, 2021
De novo missense variants in FBXO11 alter its protein expression and subcellular localization
Anne Gregor, Tanja Meerbrei, Thorsten Gerstner, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 19, 2022
First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease
Matina Prapa, Mauro Lago-Docampo, Emilia M Swietlik, et al.
American Journal of Human Genetics
|
July 31, 2018
De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder
Anne Gregor, Lynette G Sadleir, Reza Asadollahi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2022
Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia
Heba Morsy, Mehdi Benkirane, Elisa Cali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 14, 2024
Upregulation versus loss of function of NTRK2 in 44 affected individuals leads to 2 distinct neurodevelopmental disorders
Eva Berger, Robin-Tobias Jauss, Judith D Ranells, et al.
Multiple Sclerosis and Related Disorders
|
July 7, 2020
Treatment of MOG-IgG-associated disorder with rituximab: An international study of 121 patients
Daniel H Whittam, Alvaro Cobo-Calvo, A Sebastian Lopez-Chiriboga, et al.
Journal of Medical Genetics
|
November 4, 2017
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
Margot R F Reijnders, Robert Janowski, Mohsan Alvi, et al.
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of 19
Search research articles
Search
Showing results (161-170 of 182) with videos related to
Sort By:
Page
of 19
Nature Genetics
|
October 27, 2014
Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy
Carol-Anne Martin, Ilyas Ahmad, Anna Klingseisen, et al.
Human Mutation
|
June 18, 2019
Deleterious de novo variants of X-linked ZC4H2 in females cause a variable phenotype with neurogenic arthrogryposis multiplex congenita
Suzanna G M Frints, Friederike Hennig, Roberto Colombo, et al.
European Heart Journal
|
May 28, 2024
Atherosclerosis in ancient mummified humans: the global HORUS study
Randall C Thompson, M Linda Sutherland, Adel H Allam, et al.
Human Molecular Genetics
|
September 10, 2021
De novo missense variants in FBXO11 alter its protein expression and subcellular localization
Anne Gregor, Tanja Meerbrei, Thorsten Gerstner, et al.
American Journal of Respiratory and Critical Care Medicine
|
July 19, 2022
First Genotype-Phenotype Study in TBX4 Syndrome: Gain-of-Function Mutations Causative for Lung Disease
Matina Prapa, Mauro Lago-Docampo, Emilia M Swietlik, et al.
American Journal of Human Genetics
|
July 31, 2018
De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder
Anne Gregor, Lynette G Sadleir, Reza Asadollahi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2022
Expanding SPTAN1 monoallelic variant associated disorders: From epileptic encephalopathy to pure spastic paraplegia and ataxia
Heba Morsy, Mehdi Benkirane, Elisa Cali, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 14, 2024
Upregulation versus loss of function of NTRK2 in 44 affected individuals leads to 2 distinct neurodevelopmental disorders
Eva Berger, Robin-Tobias Jauss, Judith D Ranells, et al.
Multiple Sclerosis and Related Disorders
|
July 7, 2020
Treatment of MOG-IgG-associated disorder with rituximab: An international study of 121 patients
Daniel H Whittam, Alvaro Cobo-Calvo, A Sebastian Lopez-Chiriboga, et al.
Journal of Medical Genetics
|
November 4, 2017
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature
Margot R F Reijnders, Robert Janowski, Mohsan Alvi, et al.
Page
of 19