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Plos Neglected Tropical Diseases
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July 29, 2024
Could prophylactic antivirals reduce dengue incidence in a high-prevalence endemic area?
Yalda Jafari, Oliver J Brady, Joseph R Biggs, et al.
Investigative Ophthalmology & Visual Science
|
October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations
Barbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Human Molecular Genetics
|
September 28, 2011
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes
Wen Li, Xianming Wang, Wenxia Fan, et al.
Journal of Medical Genetics
|
October 17, 2009
Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome
Bernard Thienpont, Frédérique Béna, Jeroen Breckpot, et al.
The New England Journal of Medicine
|
March 16, 2017
Short-Course Radiation plus Temozolomide in Elderly Patients with Glioblastoma
James R Perry, Normand Laperriere, Christopher J O'Callaghan, et al.
European Journal of Cancer (Oxford, England : 1990)
|
November 19, 2021
The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples
Ruben Van Paemel, Charlotte Vandeputte, Lennart Raman, et al.
Nature Communications
|
October 23, 2019
A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation
S J Tavernier, V Athanasopoulos, P Verloo, et al.
The New England Journal of Medicine
|
March 11, 2016
Four Artemisinin-Based Treatments in African Pregnant Women with Malaria
, Divine Pekyi, Akua A Ampromfi, et al.
Nature Communications
|
November 21, 2019
Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation
S J Tavernier, V Athanasopoulos, P Verloo, et al.
Prenatal Diagnosis
|
May 22, 2020
Prenatally detected copy number variants in a national cohort: A postnatal follow-up study
Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, et al.
Page
of 58
Search research articles
Search
Showing results (531-540 of 571) with videos related to
Sort By:
Page
of 58
Plos Neglected Tropical Diseases
|
July 29, 2024
Could prophylactic antivirals reduce dengue incidence in a high-prevalence endemic area?
Yalda Jafari, Oliver J Brady, Joseph R Biggs, et al.
Investigative Ophthalmology & Visual Science
|
October 1, 2010
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations
Barbara D'haene, Françoise Meire, Ilse Claerhout, et al.
Human Molecular Genetics
|
September 28, 2011
Modeling abnormal early development with induced pluripotent stem cells from aneuploid syndromes
Wen Li, Xianming Wang, Wenxia Fan, et al.
Journal of Medical Genetics
|
October 17, 2009
Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome
Bernard Thienpont, Frédérique Béna, Jeroen Breckpot, et al.
The New England Journal of Medicine
|
March 16, 2017
Short-Course Radiation plus Temozolomide in Elderly Patients with Glioblastoma
James R Perry, Normand Laperriere, Christopher J O'Callaghan, et al.
European Journal of Cancer (Oxford, England : 1990)
|
November 19, 2021
The feasibility of using liquid biopsies as a complementary assay for copy number aberration profiling in routinely collected paediatric cancer patient samples
Ruben Van Paemel, Charlotte Vandeputte, Lennart Raman, et al.
Nature Communications
|
October 23, 2019
A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation
S J Tavernier, V Athanasopoulos, P Verloo, et al.
The New England Journal of Medicine
|
March 11, 2016
Four Artemisinin-Based Treatments in African Pregnant Women with Malaria
, Divine Pekyi, Akua A Ampromfi, et al.
Nature Communications
|
November 21, 2019
Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation
S J Tavernier, V Athanasopoulos, P Verloo, et al.
Prenatal Diagnosis
|
May 22, 2020
Prenatally detected copy number variants in a national cohort: A postnatal follow-up study
Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, et al.
Page
of 58