Search research articles
Contact Us
Filters
Showing results (531-540 of 637) with videos related to
Page
of 64
Sort By:
Annals of Human Genetics
|
February 4, 2022
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing
Ashraf Yahia, Ikhlas Ben Ayed, Ahlam A Hamed, et al.
Brain : a Journal of Neurology
|
May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegia
Eleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Neurogenetics
|
June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome Project
Andrea Haworth, Lars Bertram, Paola Carrera, et al.
EMBO Molecular Medicine
|
November 28, 2024
Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome
Efil Bayam, Peggy Tilly, Stephan C Collins, et al.
European Journal of Human Genetics : EJHG
|
February 5, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
Mahmoud Koko, Maha A Elseed, Inaam N Mohammed, et al.
Frontiers in Neurology
|
September 7, 2021
Pathogenic Variants in <i>ABHD16A</i> Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
Ashraf Yahia, Liena E O Elsayed, Remi Valter, et al.
Applied Optics
|
May 13, 2021
Optical wireless communication performance enhancement using Hamming coding and an efficient adaptive equalizer with a deep-learning-based quality assessment
Bidaa Mortada, Hanan S Ghanem, Randa S Hammad, et al.
Human Mutation
|
July 4, 2012
Human Variome Project country nodes: documenting genetic information within a country
George P Patrinos, Timothy D Smith, Heather Howard, et al.
La Clinica Terapeutica
|
April 3, 2025
The usability of umbilical cord blood and infant blood procalcitonin as an early diagnostic marker in diagnosing early onset bacterial sepsis to enhance antibiotic stewardship (A prospective, case-control study)
F G Yehia, H Elhakeem, E E Mohamed, et al.
European Journal of Human Genetics : EJHG
|
September 8, 2016
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan
Liena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
Page
of 64
Search research articles
Search
Showing results (531-540 of 637) with videos related to
Sort By:
Page
of 64
Annals of Human Genetics
|
February 4, 2022
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing
Ashraf Yahia, Ikhlas Ben Ayed, Ahlam A Hamed, et al.
Brain : a Journal of Neurology
|
May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegia
Eleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Neurogenetics
|
June 2, 2011
Call for participation in the neurogenetics consortium within the Human Variome Project
Andrea Haworth, Lars Bertram, Paola Carrera, et al.
EMBO Molecular Medicine
|
November 28, 2024
Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome
Efil Bayam, Peggy Tilly, Stephan C Collins, et al.
European Journal of Human Genetics : EJHG
|
February 5, 2024
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
Mahmoud Koko, Maha A Elseed, Inaam N Mohammed, et al.
Frontiers in Neurology
|
September 7, 2021
Pathogenic Variants in <i>ABHD16A</i> Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
Ashraf Yahia, Liena E O Elsayed, Remi Valter, et al.
Applied Optics
|
May 13, 2021
Optical wireless communication performance enhancement using Hamming coding and an efficient adaptive equalizer with a deep-learning-based quality assessment
Bidaa Mortada, Hanan S Ghanem, Randa S Hammad, et al.
Human Mutation
|
July 4, 2012
Human Variome Project country nodes: documenting genetic information within a country
George P Patrinos, Timothy D Smith, Heather Howard, et al.
La Clinica Terapeutica
|
April 3, 2025
The usability of umbilical cord blood and infant blood procalcitonin as an early diagnostic marker in diagnosing early onset bacterial sepsis to enhance antibiotic stewardship (A prospective, case-control study)
F G Yehia, H Elhakeem, E E Mohamed, et al.
European Journal of Human Genetics : EJHG
|
September 8, 2016
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan
Liena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, et al.
Page
of 64