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Blood Advances|May 30, 2017
The clinical spectrum of Erdheim-Chester disease: an observational cohort studyJuvianee I Estrada-Veras, Kevin J O'Brien, Louisa C Boyd, et al.
Nature Communications|October 13, 2019
Contribution of retrotransposition to developmental disordersEugene J Gardner, Elena Prigmore, Giuseppe Gallone, et al.
Nature Communications|January 28, 2021
The contribution of X-linked coding variation to severe developmental disordersHilary C Martin, Eugene J Gardner, Kaitlin E Samocha, et al.
Melanoma Research|August 12, 2017
Risk factors for development of melanoma brain metastasis and disease progression: a single-center retrospective analysisLaura J Gardner, Morgan Ward, Robert H I Andtbacka, et al.
Human Molecular Genetics|August 13, 2003
Claudin 14 knockout mice, a model for autosomal recessive deafness DFNB29, are deaf due to cochlear hair cell degenerationTamar Ben-Yosef, Inna A Belyantseva, Thomas L Saunders, et al.
Nature|October 9, 2002
A proteomic view of the Plasmodium falciparum life cycleLaurence Florens, Michael P Washburn, J Dale Raine, et al.
Cell Genomics|August 21, 2023
Large-scale exome sequence analysis identifies sex- and age-specific determinants of obesityLena R Kaisinger, Katherine A Kentistou, Stasa Stankovic, et al.
American Journal of Human Genetics|April 28, 2001
Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANKE Reichenberger, V Tiziani, S Watanabe, et al.
International Journal of Gynecological Cancer : Official Journal of the International Gynecological Cancer Society|March 21, 2024
ARIA II: a randomized controlled trial of near-infrared Angiography during RectosIgmoid resection and Anastomosis in women with ovarian cancerMario M Leitao, Alexia Iasonos, Morgan Tomberlin, et al.
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