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Psychiatry Research
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March 23, 2019
DGCR2 influences cortical thickness through a mechanism independent of schizophrenia pathogenesis
Sintia Iole Belangero, Vanessa Kiyomi Ota, Ary Gadelha, et al.
Molecular Syndromology
|
February 12, 2026
Genotype-Phenotype Analysis and New Clinical Findings in a Series of 24 Patients Presenting with Noonan Syndrome and Related Disorders
Bruna Miranda Corso, Luiza de Oliveira Simões, Karina Montemor Klegen de Oliveira, et al.
Clinical Genetics
|
June 12, 2025
Clinical and Molecular Characterization of Xia-Gibbs Syndrome: Expanding the Phenotypic Spectrum in a Brazilian Cohort
Maísa Ganz Sanchez Sennes, Laura Machado Lara Carvalho, Matheus Augusto Araújo Castro, et al.
Human Mutation
|
December 2, 2017
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
Mariana Moysés-Oliveira, Giuliana Giannuzzi, Richard J Fish, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Research Square
|
June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
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Search research articles
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Showing results (81-90 of 86) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 86 results.
Psychiatry Research
|
March 23, 2019
DGCR2 influences cortical thickness through a mechanism independent of schizophrenia pathogenesis
Sintia Iole Belangero, Vanessa Kiyomi Ota, Ary Gadelha, et al.
Molecular Syndromology
|
February 12, 2026
Genotype-Phenotype Analysis and New Clinical Findings in a Series of 24 Patients Presenting with Noonan Syndrome and Related Disorders
Bruna Miranda Corso, Luiza de Oliveira Simões, Karina Montemor Klegen de Oliveira, et al.
Clinical Genetics
|
June 12, 2025
Clinical and Molecular Characterization of Xia-Gibbs Syndrome: Expanding the Phenotypic Spectrum in a Brazilian Cohort
Maísa Ganz Sanchez Sennes, Laura Machado Lara Carvalho, Matheus Augusto Araújo Castro, et al.
Human Mutation
|
December 2, 2017
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
Mariana Moysés-Oliveira, Giuliana Giannuzzi, Richard J Fish, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Research Square
|
June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
Hellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
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of 9