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American Journal of Medical Genetics. Part A|January 4, 2023
A biallelic frameshift indel in PPP1R35 as a cause of primary microcephalyMoez Dawood, Gulsen Akay, Tadahiro Mitani, et al.
Neurology. Genetics|June 24, 2022
Genome Sequencing in the Parkinson Disease ClinicEmily J Hill, Laurie A Robak, Rami Al-Ouran, et al.
Journal of the National Cancer Institute|December 29, 2020
Germline Cancer Predisposition Variants in Pediatric Rhabdomyosarcoma: A Report From the Children's Oncology GroupHe Li, Saumya D Sisoudiya, Bailey A Martin-Giacalone, et al.
Genetics in Medicine Open|December 13, 2024
The impact of the Turkish population variome on the genomic architecture of rare disease traitsZeynep Coban-Akdemir, Xiaofei Song, Francisco C Ceballos, et al.
HGG Advances|December 24, 2021
<i>AHDC1</i> missense mutations in Xia-Gibbs syndromeMichael M Khayat, Jianhong Hu, Yunyun Jiang, et al.
Science (New York, N.Y.)|March 24, 2000
A BAC-based physical map of the major autosomes of Drosophila melanogasterR A Hoskins, C R Nelson, B P Berman, et al.
Journal of Bacteriology|August 20, 2004
Complete genome sequence of Rickettsia typhi and comparison with sequences of other rickettsiaeMichael P McLeod, Xiang Qin, Sandor E Karpathy, et al.
The New England Journal of Medicine|March 12, 2010
Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathyJames R Lupski, Jeffrey G Reid, Claudia Gonzaga-Jauregui, et al.
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