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American Journal of Medical Genetics. Part A
|
May 4, 2011
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment
Nanna D Rendtorff, Marianne Lodahl, Houda Boulahbel, et al.
American Journal of Human Genetics
|
July 9, 2013
Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability
Nina Bögershausen, Nassim Shahrzad, Jessica X Chong, et al.
JAMA Oncology
|
February 28, 2020
Global Retinoblastoma Presentation and Analysis by National Income Level
, Ido Didi Fabian, Elhassan Abdallah, et al.
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of 5
Search research articles
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Showing results (41-50 of 43) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 43 results.
American Journal of Medical Genetics. Part A
|
May 4, 2011
Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment
Nanna D Rendtorff, Marianne Lodahl, Houda Boulahbel, et al.
American Journal of Human Genetics
|
July 9, 2013
Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability
Nina Bögershausen, Nassim Shahrzad, Jessica X Chong, et al.
JAMA Oncology
|
February 28, 2020
Global Retinoblastoma Presentation and Analysis by National Income Level
, Ido Didi Fabian, Elhassan Abdallah, et al.
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of 5