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Nature Communications
|
June 19, 2021
Engineering an anti-HER2 biparatopic antibody with a multimodal mechanism of action
Florian Kast, Martin Schwill, Jakob C Stüber, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy
Henrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Acta Neuropathologica Communications
|
November 22, 2023
Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families
Christine A M Weber, Nicole Krönke, Valery Volk, et al.
Infection Control and Hospital Epidemiology
|
August 11, 2011
Clostridium difficile outbreak strain BI is highly endemic in Chicago area hospitals
Stephanie R Black, Kingsley N Weaver, Roderick C Jones, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery
|
March 21, 2014
Update with level 1 studies of the European Hernia Society guidelines on the treatment of inguinal hernia in adult patients
M Miserez, E Peeters, T Aufenacker, et al.
European Journal of Human Genetics : EJHG
|
August 2, 2020
Rare heterozygous GDF6 variants in patients with renal anomalies
Helge Martens, Imke Hennies, Maike Getwan, et al.
Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2001
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches
A Corrias, S Einaudi, E Chiorboli, et al.
Human Genetics
|
November 18, 2015
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)
Anne Kosfeld, Martin Kreuzer, Christoph Daniel, et al.
European Journal of Human Genetics : EJHG
|
July 31, 2019
Assessment of genetic variant burden in epilepsy-associated brain lesions
Lisa-Marie Niestroj, Patrick May, Mykyta Artomov, et al.
Page
of 138
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Showing results (1141-1150 of 1,377) with videos related to
Sort By:
Page
of 138
Nature Communications
|
June 19, 2021
Engineering an anti-HER2 biparatopic antibody with a multimodal mechanism of action
Florian Kast, Martin Schwill, Jakob C Stüber, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 7, 2019
Targeted gene sequencing in 6994 individuals with neurodevelopmental disorder with epilepsy
Henrike O Heyne, Mykyta Artomov, Florian Battke, et al.
Acta Neuropathologica Communications
|
November 22, 2023
Rare germline variants in POLE and POLD1 encoding the catalytic subunits of DNA polymerases ε and δ in glioma families
Christine A M Weber, Nicole Krönke, Valery Volk, et al.
Infection Control and Hospital Epidemiology
|
August 11, 2011
Clostridium difficile outbreak strain BI is highly endemic in Chicago area hospitals
Stephanie R Black, Kingsley N Weaver, Roderick C Jones, et al.
Hernia : the Journal of Hernias and Abdominal Wall Surgery
|
March 21, 2014
Update with level 1 studies of the European Hernia Society guidelines on the treatment of inguinal hernia in adult patients
M Miserez, E Peeters, T Aufenacker, et al.
European Journal of Human Genetics : EJHG
|
August 2, 2020
Rare heterozygous GDF6 variants in patients with renal anomalies
Helge Martens, Imke Hennies, Maike Getwan, et al.
Annals of Neurology
|
October 3, 2009
Early-onset absence epilepsy caused by mutations in the glucose transporter GLUT1
Arvid Suls, Saul A Mullen, Yvonne G Weber, et al.
The Journal of Clinical Endocrinology and Metabolism
|
October 16, 2001
Accuracy of fine needle aspiration biopsy of thyroid nodules in detecting malignancy in childhood: comparison with conventional clinical, laboratory, and imaging approaches
A Corrias, S Einaudi, E Chiorboli, et al.
Human Genetics
|
November 18, 2015
Whole-exome sequencing identifies mutations of TBC1D1 encoding a Rab-GTPase-activating protein in patients with congenital anomalies of the kidneys and urinary tract (CAKUT)
Anne Kosfeld, Martin Kreuzer, Christoph Daniel, et al.
European Journal of Human Genetics : EJHG
|
July 31, 2019
Assessment of genetic variant burden in epilepsy-associated brain lesions
Lisa-Marie Niestroj, Patrick May, Mykyta Artomov, et al.
Page
of 138