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Pediatric Neurology
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November 5, 2021
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome
Jacqueline L Steele, Michelle M Morrow, Harvey B Sarnat, et al.
American Journal of Human Genetics
|
October 26, 2023
An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP
Annelise Y Mah-Som, Jil Daw, Diana Huynh, et al.
Genome Medicine
|
December 19, 2024
Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression
Davut Pehlivan, Jesse D Bengtsson, Sameer S Bajikar, et al.
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Search research articles
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Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 13 results.
Pediatric Neurology
|
November 5, 2021
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome
Jacqueline L Steele, Michelle M Morrow, Harvey B Sarnat, et al.
American Journal of Human Genetics
|
October 26, 2023
An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP
Annelise Y Mah-Som, Jil Daw, Diana Huynh, et al.
Genome Medicine
|
December 19, 2024
Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression
Davut Pehlivan, Jesse D Bengtsson, Sameer S Bajikar, et al.
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of 2