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Cancer
|
April 7, 2018
CNS Langerhans cell histiocytosis: Common hematopoietic origin for LCH-associated neurodegeneration and mass lesions
Kenneth L McClain, Jennifer Picarsic, Rikhia Chakraborty, et al.
Nature Genetics
|
April 21, 2015
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis
Levi B Watkin, Birthe Jessen, Wojciech Wiszniewski, et al.
American Journal of Human Genetics
|
August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay
Ronit Marom, Lindsay C Burrage, Rossella Venditti, et al.
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of 27
Search research articles
Search
Showing results (261-270 of 263) with videos related to
Sort By:
Page
of 27
You have reached the last page of results.
This site can display upto 263 results.
Cancer
|
April 7, 2018
CNS Langerhans cell histiocytosis: Common hematopoietic origin for LCH-associated neurodegeneration and mass lesions
Kenneth L McClain, Jennifer Picarsic, Rikhia Chakraborty, et al.
Nature Genetics
|
April 21, 2015
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis
Levi B Watkin, Birthe Jessen, Wojciech Wiszniewski, et al.
American Journal of Human Genetics
|
August 27, 2021
COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay
Ronit Marom, Lindsay C Burrage, Rossella Venditti, et al.
Page
of 27