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Pediatric Research
|
December 18, 2024
Pediatric SARS-CoV-2 long term outcomes study (PECOS): cross sectional analysis at baseline
Gina A Montealegre Sanchez, Lauren E Arrigoni, Alexandra B Yonts, et al.
Human Mutation
|
March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients
Bobby G Ng, Sergey A Shiryaev, Daisy Rymen, et al.
Human Mutation
|
March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
Bobby G Ng, Paulina Sosicka, Satish Agadi, et al.
American Journal of Human Genetics
|
January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Joery den Hoed, Elke de Boer, Norine Voisin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disorders
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature
|
July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Science Advances
|
December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients
Laura Bryant, Dong Li, Samuel G Cox, et al.
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Search research articles
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Showing results (171-180 of 177) with videos related to
Sort By:
Page
of 18
You have reached the last page of results.
This site can display upto 177 results.
Pediatric Research
|
December 18, 2024
Pediatric SARS-CoV-2 long term outcomes study (PECOS): cross sectional analysis at baseline
Gina A Montealegre Sanchez, Lauren E Arrigoni, Alexandra B Yonts, et al.
Human Mutation
|
March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients
Bobby G Ng, Sergey A Shiryaev, Daisy Rymen, et al.
Human Mutation
|
March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
Bobby G Ng, Paulina Sosicka, Satish Agadi, et al.
American Journal of Human Genetics
|
January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction
Joery den Hoed, Elke de Boer, Norine Voisin, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 22, 2024
<i>De novo</i> variants in the non-coding spliceosomal snRNA gene <i>RNU4-2</i> are a frequent cause of syndromic neurodevelopmental disorders
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Nature
|
July 11, 2024
De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome
Yuyang Chen, Ruebena Dawes, Hyung Chul Kim, et al.
Science Advances
|
December 3, 2020
Histone H3.3 beyond cancer: Germline mutations in <i>Histone 3 Family 3A and 3B</i> cause a previously unidentified neurodegenerative disorder in 46 patients
Laura Bryant, Dong Li, Samuel G Cox, et al.
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of 18