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American Journal of Human Genetics
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November 1, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals
Giuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 13, 2015
Clinical phenotype of the recurrent 1q21.1 copy-number variant
Raphael Bernier, Kyle J Steinman, Beau Reilly, et al.
Frontiers in Integrative Neuroscience
|
April 30, 2020
The Autism Biomarkers Consortium for Clinical Trials (ABC-CT): Scientific Context, Study Design, and Progress Toward Biomarker Qualification
James C McPartland, Raphael A Bernier, Shafali S Jeste, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 31, 2019
Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome
Pleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 24, 2018
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome
Pleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
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of 2
Search research articles
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Showing results (11-20 of 15) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 15 results.
American Journal of Human Genetics
|
November 1, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism Individuals
Giuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 13, 2015
Clinical phenotype of the recurrent 1q21.1 copy-number variant
Raphael Bernier, Kyle J Steinman, Beau Reilly, et al.
Frontiers in Integrative Neuroscience
|
April 30, 2020
The Autism Biomarkers Consortium for Clinical Trials (ABC-CT): Scientific Context, Study Design, and Progress Toward Biomarker Qualification
James C McPartland, Raphael A Bernier, Shafali S Jeste, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 31, 2019
Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome
Pleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 24, 2018
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome
Pleuntje J van der Sluijs, Sandra Jansen, Samantha A Vergano, et al.
Page
of 2