Showing results (1131-1140 of 2,519) with videos related to

Sort By:
Pageof 252
Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.
Molecular Genetics & Genomic Medicine|January 29, 2015
Performance evaluation of Sanger sequencing for the diagnosis of primary hyperoxaluria and comparison with targeted next generation sequencingEmma L Williams, Eleanor A L Bagg, Michael Mueller, et al.
Molecular Genetics & Genomic Medicine|July 18, 2022
Adults with lysosomal storage diseases in the undiagnosed diseases networkChangrui Xiao, Mary Koziura, Heidi Cope, et al.
Molecular Genetics & Genomic Medicine|May 15, 2023
A case of infantile Barth syndrome with severe heart failure: Importance of splicing variants in the TAZ geneAtsuhito Takeda, Masahiro Ueki, Jiro Abe, et al.
Molecular Genetics & Genomic Medicine|February 15, 2023
Whole-exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseasesStefania Lenarduzzi, Beatrice Spedicati, Beatrice Alessandrini, et al.
Molecular Genetics & Genomic Medicine|February 22, 2023
Novel IRF6 variant in orofacial cleft patients from Durban, South AfricaThirona Naicker, Azeez Alade, Chinyere Adeleke, et al.
Molecular Genetics & Genomic Medicine|March 3, 2023
Expanding the genetic spectrum of giant axonal neuropathy: Two novel variants in Iranian familiesMahmoud Reza Ashrafi, Ali Zare Dehnavi, Ali Reza Tavasoli, et al.
Molecular Genetics & Genomic Medicine|March 19, 2023
Genetic analysis of periventricular nodular heterotopia 7 caused by a novel NEDD4L missense mutation: Case and literature summaryJuan Liu, Jihong Hu, Yaqing Duan, et al.
Molecular Genetics & Genomic Medicine|August 24, 2021
Prevalence of Y chromosome microdeletion in azoospermia factor subregions among infertile men from West Bengal, IndiaSaurav Dutta, Pranab Paladhi, Samudra Pal, et al.
Molecular Genetics & Genomic Medicine|August 10, 2022
Distribution and transmission of copy number variations of uncertain significance in 105 triosQiang Wen, Xiu Wang, Hao Zhang, et al.
Pageof 252