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Amira Nabil

Showing results (11-20 of 17) with videos related to

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Frontiers in Immunology|October 10, 2022
Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritisHeba R Gouda, Iman M Talaat, Amal Bouzid, et al.
Clinical Genetics|April 30, 2025
Analysis of Copy Number Variants Is an Important Consideration in Exome SequencingAsmaa K Amin, Sara H El-Dessouky, Marwa Abd Elmaksoud, et al.
Brain : a Journal of Neurology|April 14, 2020
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathyNicolas Chatron, Felicitas Becker, Heba Morsy, et al.
American Journal of Human Genetics|January 22, 2026
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathyHeba Morsy, Hyeonho Kim, Gyubin Jang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2018
Expanding the phenome and variome of skeletal dysplasiaSateesh Maddirevula, Saud Alsahli, Lamees Alhabeeb, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Frontiers in Immunology|October 10, 2022
Genetic analysis of CFH and MCP in Egyptian patients with immune-complex proliferative glomerulonephritisHeba R Gouda, Iman M Talaat, Amal Bouzid, et al.
Clinical Genetics|April 30, 2025
Analysis of Copy Number Variants Is an Important Consideration in Exome SequencingAsmaa K Amin, Sara H El-Dessouky, Marwa Abd Elmaksoud, et al.
Brain : a Journal of Neurology|April 14, 2020
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathyNicolas Chatron, Felicitas Becker, Heba Morsy, et al.
American Journal of Human Genetics|January 22, 2026
MDGA2 homozygous loss-of-function variants cause developmental and epileptic encephalopathyHeba Morsy, Hyeonho Kim, Gyubin Jang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 6, 2018
Expanding the phenome and variome of skeletal dysplasiaSateesh Maddirevula, Saud Alsahli, Lamees Alhabeeb, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
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