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Ebiomedicine
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January 7, 2024
Metabolite profiles of medulloblastoma for rapid and non-invasive detection of molecular disease groups
Sarah Kohe, Christopher Bennett, Florence Burté, et al.
American Journal of Human Genetics
|
August 5, 2008
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
Vincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, et al.
Nature Genetics
|
April 24, 2012
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan
Tony Roscioli, Erik-Jan Kamsteeg, Karen Buysse, et al.
European Journal of Human Genetics : EJHG
|
December 1, 2011
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum
Siddharth Banka, Ratna Veeramachaneni, William Reardon, et al.
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of 5
Search research articles
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Showing results (41-50 of 44) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 44 results.
Ebiomedicine
|
January 7, 2024
Metabolite profiles of medulloblastoma for rapid and non-invasive detection of molecular disease groups
Sarah Kohe, Christopher Bennett, Florence Burté, et al.
American Journal of Human Genetics
|
August 5, 2008
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome
Vincent Cantagrel, Jennifer L Silhavy, Stephanie L Bielas, et al.
Nature Genetics
|
April 24, 2012
Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan
Tony Roscioli, Erik-Jan Kamsteeg, Karen Buysse, et al.
European Journal of Human Genetics : EJHG
|
December 1, 2011
How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum
Siddharth Banka, Ratna Veeramachaneni, William Reardon, et al.
Page
of 5