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Journal of Comparative Effectiveness Research
|
March 12, 2026
A novel real-world data methodology for lymphoma outcome classification: the real-world Lugano study
Richard Scott Swain, Andrew Klink, Parisa Asgarisabet, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2016
Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findings
Madeleine Tooley, Danielle Lynch, Francois Bernier, et al.
American Journal of Obstetrics and Gynecology
|
December 18, 2025
Preimplantation genetic testing for aneuploidy mosaicism reporting lacks clinical predictive value for live birth in a multisite, double-blinded study with independent validation
Pavan Gill, Xin Tao, Yiping Zhan, et al.
Pharmacogenomics
|
October 8, 2004
Biomedical informatics: development of a comprehensive data warehouse for clinical and genomic breast cancer research
Hai Hu, Henry Brzeski, Joe Hutchins, et al.
European Journal of Human Genetics : EJHG
|
October 4, 2012
Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A
Eyal Reinstein, Sophia Frentz, Tim Morgan, et al.
Molecular Human Reproduction
|
June 4, 2016
The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists
Karen Sermon, Antonio Capalbo, Jacques Cohen, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
May 7, 2026
Clinicians' attitudes to evolutionary versus genetic explanations for anxiety: cluster-randomised study of stigmatisation
Adam D Hunt, Tom Carpenter, Gurjot Brar, et al.
Human Molecular Genetics
|
March 21, 2020
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome
Reham Alharatani, Athina Ververi, Ana Beleza-Meireles, et al.
American Journal of Human Genetics
|
December 14, 2011
Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity
Eric D Boyden, A Belinda Campos-Xavier, Sebastian Kalamajski, et al.
American Journal of Human Genetics
|
December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome
Anna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
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of 18
Search research articles
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Showing results (161-170 of 176) with videos related to
Sort By:
Page
of 18
Journal of Comparative Effectiveness Research
|
March 12, 2026
A novel real-world data methodology for lymphoma outcome classification: the real-world Lugano study
Richard Scott Swain, Andrew Klink, Parisa Asgarisabet, et al.
American Journal of Medical Genetics. Part A
|
March 15, 2016
Cerebro-costo-mandibular syndrome: Clinical, radiological, and genetic findings
Madeleine Tooley, Danielle Lynch, Francois Bernier, et al.
American Journal of Obstetrics and Gynecology
|
December 18, 2025
Preimplantation genetic testing for aneuploidy mosaicism reporting lacks clinical predictive value for live birth in a multisite, double-blinded study with independent validation
Pavan Gill, Xin Tao, Yiping Zhan, et al.
Pharmacogenomics
|
October 8, 2004
Biomedical informatics: development of a comprehensive data warehouse for clinical and genomic breast cancer research
Hai Hu, Henry Brzeski, Joe Hutchins, et al.
European Journal of Human Genetics : EJHG
|
October 4, 2012
Vascular and connective tissue anomalies associated with X-linked periventricular heterotopia due to mutations in Filamin A
Eyal Reinstein, Sophia Frentz, Tim Morgan, et al.
Molecular Human Reproduction
|
June 4, 2016
The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists
Karen Sermon, Antonio Capalbo, Jacques Cohen, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
May 7, 2026
Clinicians' attitudes to evolutionary versus genetic explanations for anxiety: cluster-randomised study of stigmatisation
Adam D Hunt, Tom Carpenter, Gurjot Brar, et al.
Human Molecular Genetics
|
March 21, 2020
Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome
Reham Alharatani, Athina Ververi, Ana Beleza-Meireles, et al.
American Journal of Human Genetics
|
December 14, 2011
Recurrent dominant mutations affecting two adjacent residues in the motor domain of the monomeric kinesin KIF22 result in skeletal dysplasia and joint laxity
Eric D Boyden, A Belinda Campos-Xavier, Sebastian Kalamajski, et al.
American Journal of Human Genetics
|
December 3, 2014
Mutations in SNX14 cause a distinctive autosomal-recessive cerebellar ataxia and intellectual disability syndrome
Anna C Thomas, Hywel Williams, Núria Setó-Salvia, et al.
Page
of 18