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Showing results (611-620 of 614) with videos related to

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Nature|March 27, 2025
The contribution of de novo coding mutations to meningomyeloceleYoo-Jin Jiny Ha, Ashna Nisal, Isaac Tang, et al.
Science (New York, N.Y.)|May 2, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletionKeng Ioi Vong, Sangmoon Lee, Kit Sing Au, et al.
American Journal of Human Genetics|April 19, 2016
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis VariantJun Li, Susan L Woods, Sue Healey, et al.
Human Molecular Genetics|July 17, 2014
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Zhaoming Wang, Bin Zhu, Mingfeng Zhang, et al.
Pageof 62

Showing results (611-620 of 614) with videos related to

Sort By:
Pageof 62
You have reached the last page of results.This site can display upto 614 results.
Nature|March 27, 2025
The contribution of de novo coding mutations to meningomyeloceleYoo-Jin Jiny Ha, Ashna Nisal, Isaac Tang, et al.
Science (New York, N.Y.)|May 2, 2024
Risk of meningomyelocele mediated by the common 22q11.2 deletionKeng Ioi Vong, Sangmoon Lee, Kit Sing Au, et al.
American Journal of Human Genetics|April 19, 2016
Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis VariantJun Li, Susan L Woods, Sue Healey, et al.
Human Molecular Genetics|July 17, 2014
Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Zhaoming Wang, Bin Zhu, Mingfeng Zhang, et al.
Pageof 62