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International Journal of Molecular Sciences
|
November 27, 2021
The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model
Katherine C MacKenzie, Rhiana Garritsen, Rajendra K Chauhan, et al.
Nature Communications
|
March 31, 2026
CXCR3 is associated with T-cell-induced heart damage in acute rheumatic fever
Francis M Middleton, Reuben McGregor, Natalie Lorenz, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
December 21, 2023
ATP5PO levels regulate enteric nervous system development in zebrafish, linking Hirschsprung disease to Down Syndrome
L E Kuil, R K Chauhan, B M de Graaf, et al.
JAMA Neurology
|
January 27, 2015
Factors associated with the onset and persistence of post-lumbar puncture headache
Andrés E Monserrate, Davis C Ryman, Shengmei Ma, et al.
JCI Insight
|
March 22, 2024
Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome
Avinaash V Maharaj, Emily Cottrell, Thatchawan Thanasupawat, et al.
Annals of Clinical Microbiology and Antimicrobials
|
April 20, 2025
Long COVID clinical evaluation, research and impact on society: a global expert consensus
Andrew G Ewing, David Joffe, Svetlana Blitshteyn, et al.
Human Molecular Genetics
|
December 10, 2015
ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
Danny Halim, Robert M W Hofstra, Luca Signorile, et al.
Trends in Ecology & Evolution
|
July 16, 2018
Did Our Species Evolve in Subdivided Populations across Africa, and Why Does It Matter?
Eleanor M L Scerri, Mark G Thomas, Andrea Manica, et al.
Human Mutation
|
September 17, 2020
Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP
Katherine C MacKenzie, Bianca M de Graaf, Andreas Syrimis, et al.
Acta Obstetricia Et Gynecologica Scandinavica
|
November 29, 2020
The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies
Karin E M Diderich, Kathleen Romijn, Marieke Joosten, et al.
Page
of 73
Search research articles
Search
Showing results (651-660 of 728) with videos related to
Sort By:
Page
of 73
International Journal of Molecular Sciences
|
November 27, 2021
The Somatic Mutation Paradigm in Congenital Malformations: Hirschsprung Disease as a Model
Katherine C MacKenzie, Rhiana Garritsen, Rajendra K Chauhan, et al.
Nature Communications
|
March 31, 2026
CXCR3 is associated with T-cell-induced heart damage in acute rheumatic fever
Francis M Middleton, Reuben McGregor, Natalie Lorenz, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease
|
December 21, 2023
ATP5PO levels regulate enteric nervous system development in zebrafish, linking Hirschsprung disease to Down Syndrome
L E Kuil, R K Chauhan, B M de Graaf, et al.
JAMA Neurology
|
January 27, 2015
Factors associated with the onset and persistence of post-lumbar puncture headache
Andrés E Monserrate, Davis C Ryman, Shengmei Ma, et al.
JCI Insight
|
March 22, 2024
Characterization of HMGA2 variants expands the spectrum of Silver-Russell syndrome
Avinaash V Maharaj, Emily Cottrell, Thatchawan Thanasupawat, et al.
Annals of Clinical Microbiology and Antimicrobials
|
April 20, 2025
Long COVID clinical evaluation, research and impact on society: a global expert consensus
Andrew G Ewing, David Joffe, Svetlana Blitshteyn, et al.
Human Molecular Genetics
|
December 10, 2015
ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
Danny Halim, Robert M W Hofstra, Luca Signorile, et al.
Trends in Ecology & Evolution
|
July 16, 2018
Did Our Species Evolve in Subdivided Populations across Africa, and Why Does It Matter?
Eleanor M L Scerri, Mark G Thomas, Andrea Manica, et al.
Human Mutation
|
September 17, 2020
Goldberg-Shprintzen syndrome is determined by the absence, or reduced expression levels, of KIFBP
Katherine C MacKenzie, Bianca M de Graaf, Andreas Syrimis, et al.
Acta Obstetricia Et Gynecologica Scandinavica
|
November 29, 2020
The potential diagnostic yield of whole exome sequencing in pregnancies complicated by fetal ultrasound anomalies
Karin E M Diderich, Kathleen Romijn, Marieke Joosten, et al.
Page
of 73