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Showing results (751-760 of 756) with videos related to

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EMBO Molecular Medicine|August 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disordersSara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
Human Molecular Genetics|August 8, 2023
Macrocephaly and developmental delay caused by missense variants in RAB5CKlaas Koop, Weimin Yuan, Federico Tessadori, et al.
Hormone Research in Paediatrics|July 19, 2019
Use of Gonadotropin-Releasing Hormone Analogs in Children: Update by an International ConsortiumKanthi Bangalore Krishna, John S Fuqua, Alan D Rogol, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Nature Communications|September 10, 2024
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviorsJana Willim, Daniel Woike, Daniel Greene, et al.
Science (New York, N.Y.)|October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiCFlorian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
Pageof 76

Showing results (751-760 of 756) with videos related to

Sort By:
Pageof 76
You have reached the last page of results.This site can display upto 756 results.
EMBO Molecular Medicine|August 26, 2025
Dominant negative ATP5F1A variants disrupt oxidative phosphorylation causing neurological disordersSara M Fielder, Marisa W Friederich, Daniella H Hock, et al.
Human Molecular Genetics|August 8, 2023
Macrocephaly and developmental delay caused by missense variants in RAB5CKlaas Koop, Weimin Yuan, Federico Tessadori, et al.
Hormone Research in Paediatrics|July 19, 2019
Use of Gonadotropin-Releasing Hormone Analogs in Children: Update by an International ConsortiumKanthi Bangalore Krishna, John S Fuqua, Alan D Rogol, et al.
American Journal of Human Genetics|January 29, 2025
Sequence variants in HECTD1 result in a variable neurodevelopmental disorderGazelle Zerafati-Jahromi, Elias Oxman, Hieu D Hoang, et al.
Nature Communications|September 10, 2024
Variants in LRRC7 lead to intellectual disability, autism, aggression and abnormal eating behaviorsJana Willim, Daniel Woike, Daniel Greene, et al.
Science (New York, N.Y.)|October 31, 2024
Brain malformations and seizures by impaired chaperonin function of TRiCFlorian Kraft, Piere Rodriguez-Aliaga, Weimin Yuan, et al.
Pageof 76