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Journal of Medical Genetics
|
January 26, 2017
<i>STAG1</i> mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability
Daphné Lehalle, Anne-Laure Mosca-Boidron, Amber Begtrup, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 5, 2017
CORRIGENDUM: The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations
Chun-An Chen, Daniëlle G M Bosch, Megan T Cho ScM, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 13, 2024
How to make land use policy decisions: Integrating science and economics to deliver connected climate, biodiversity, and food objectives
Ian J Bateman, Amy Binner, Ethan T Addicott, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
November 1, 1982
[Comparative study of the effectiveness of 9,3"-di-O-acetyl midecamycin (MOM) and josamycin (JM) against acute tonsillitis by double blind method]
K Nakagawa, M Koyama, A Saito, et al.
Cell
|
February 24, 2018
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures
Vincenzo A Gennarino, Elizabeth E Palmer, Laura M McDonell, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
November 1, 1982
[Comparative study of the effectiveness of 9,33"-diacetylmidecamycin (MOM) and midecamycin on respiratory tract infection]
K Hara, K Izumikawa, M Komori, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 5, 2025
A Translational Neuroscience & Computational Evaluation of a D1R Partial Agonist for Schizophrenia (TRANSCENDS): Rationale and Study Design of a Brain-Based Clinical Trial
Clara Fonteneau, Zailyn Tamayo, Ally Price, et al.
American Journal of Human Genetics
|
April 2, 2019
De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome
Elizabeth E Palmer, Seungbeom Hong, Fatema Al Zahrani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 20, 2016
The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families
Michael D Fountain, Emmelien Aten, Megan T Cho, et al.
Journal of Psychiatric Research
|
January 10, 2026
A translational neuroscience & computational evaluation of a D1R partial agonist for schizophrenia (TRANSCENDS): Rationale and study design of a brain-based clinical trial
Clara Fonteneau, Zailyn Tamayo, Ally Price, et al.
Page
of 38
Search research articles
Search
Showing results (331-340 of 375) with videos related to
Sort By:
Page
of 38
Journal of Medical Genetics
|
January 26, 2017
<i>STAG1</i> mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability
Daphné Lehalle, Anne-Laure Mosca-Boidron, Amber Begtrup, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 5, 2017
CORRIGENDUM: The expanding clinical phenotype of Bosch-Boonstra-Schaaf optic atrophy syndrome: 20 new cases and possible genotype-phenotype correlations
Chun-An Chen, Daniëlle G M Bosch, Megan T Cho ScM, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 13, 2024
How to make land use policy decisions: Integrating science and economics to deliver connected climate, biodiversity, and food objectives
Ian J Bateman, Amy Binner, Ethan T Addicott, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
November 1, 1982
[Comparative study of the effectiveness of 9,3"-di-O-acetyl midecamycin (MOM) and josamycin (JM) against acute tonsillitis by double blind method]
K Nakagawa, M Koyama, A Saito, et al.
Cell
|
February 24, 2018
A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures
Vincenzo A Gennarino, Elizabeth E Palmer, Laura M McDonell, et al.
Kansenshogaku Zasshi. the Journal of the Japanese Association for Infectious Diseases
|
November 1, 1982
[Comparative study of the effectiveness of 9,33"-diacetylmidecamycin (MOM) and midecamycin on respiratory tract infection]
K Hara, K Izumikawa, M Komori, et al.
Medrxiv : the Preprint Server for Health Sciences
|
May 5, 2025
A Translational Neuroscience & Computational Evaluation of a D1R Partial Agonist for Schizophrenia (TRANSCENDS): Rationale and Study Design of a Brain-Based Clinical Trial
Clara Fonteneau, Zailyn Tamayo, Ally Price, et al.
American Journal of Human Genetics
|
April 2, 2019
De Novo Variants Disrupting the HX Repeat Motif of ATN1 Cause a Recognizable Non-progressive Neurocognitive Syndrome
Elizabeth E Palmer, Seungbeom Hong, Fatema Al Zahrani, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 20, 2016
The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families
Michael D Fountain, Emmelien Aten, Megan T Cho, et al.
Journal of Psychiatric Research
|
January 10, 2026
A translational neuroscience & computational evaluation of a D1R partial agonist for schizophrenia (TRANSCENDS): Rationale and study design of a brain-based clinical trial
Clara Fonteneau, Zailyn Tamayo, Ally Price, et al.
Page
of 38