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European Journal of Human Genetics : EJHG
|
July 29, 2025
Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disorders
Daphne J Smits, Christophe Debuy, Alice S Brooks, et al.
Nature Communications
|
February 10, 2026
Mutant KRAS vaccine with dual checkpoint blockade in resected pancreatic cancer: a phase I trial
Amanda L Huff, S Daniel Haldar, Alexander A Gergis, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 5, 2020
Vaccine-Induced Intratumoral Lymphoid Aggregates Correlate with Survival Following Treatment with a Neoadjuvant and Adjuvant Vaccine in Patients with Resectable Pancreatic Adenocarcinoma
Lei Zheng, Ding Ding, Barish H Edil, et al.
American Heart Journal
|
June 2, 2020
Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants
Johanna C Herkert, Judith M A Verhagen, Raquel Yotti, et al.
European Journal of Human Genetics : EJHG
|
June 10, 2010
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes
Aimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2012
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis
Sonja A de Munnik, Louise S Bicknell, Salim Aftimos, et al.
Current Biology : CB
|
April 25, 2020
Tempo and Pattern of Avian Brain Size Evolution
Daniel T Ksepka, Amy M Balanoff, N Adam Smith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype
Bertrand Isidor, Frédéric Ebstein, Anna Hurst, et al.
American Journal of Medical Genetics. Part A
|
October 2, 2012
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorder
Sonja A de Munnik, Barto J Otten, Jeroen Schoots, et al.
Science (New York, N.Y.)
|
June 10, 2017
Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade
Dung T Le, Jennifer N Durham, Kellie N Smith, et al.
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Showing results (801-810 of 821) with videos related to
Sort By:
Page
of 83
European Journal of Human Genetics : EJHG
|
July 29, 2025
Clinical utility of DNA-methylation signatures in routine diagnostics for neurodevelopmental disorders
Daphne J Smits, Christophe Debuy, Alice S Brooks, et al.
Nature Communications
|
February 10, 2026
Mutant KRAS vaccine with dual checkpoint blockade in resected pancreatic cancer: a phase I trial
Amanda L Huff, S Daniel Haldar, Alexander A Gergis, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
December 5, 2020
Vaccine-Induced Intratumoral Lymphoid Aggregates Correlate with Survival Following Treatment with a Neoadjuvant and Adjuvant Vaccine in Patients with Resectable Pancreatic Adenocarcinoma
Lei Zheng, Ding Ding, Barish H Edil, et al.
American Heart Journal
|
June 2, 2020
Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants
Johanna C Herkert, Judith M A Verhagen, Raquel Yotti, et al.
European Journal of Human Genetics : EJHG
|
June 10, 2010
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes
Aimée D C Paulussen, Constance T Schrander-Stumpel, Demis C J Tserpelis, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2012
Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication complex gene mutations and 10 without molecular diagnosis
Sonja A de Munnik, Louise S Bicknell, Salim Aftimos, et al.
Current Biology : CB
|
April 25, 2020
Tempo and Pattern of Avian Brain Size Evolution
Daniel T Ksepka, Amy M Balanoff, N Adam Smith, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype
Bertrand Isidor, Frédéric Ebstein, Anna Hurst, et al.
American Journal of Medical Genetics. Part A
|
October 2, 2012
Meier-Gorlin syndrome: growth and secondary sexual development of a microcephalic primordial dwarfism disorder
Sonja A de Munnik, Barto J Otten, Jeroen Schoots, et al.
Science (New York, N.Y.)
|
June 10, 2017
Mismatch repair deficiency predicts response of solid tumors to PD-1 blockade
Dung T Le, Jennifer N Durham, Kellie N Smith, et al.
Page
of 83