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Keyword: Whole exome sequencing
1
Pseudoileus caused by primary visceral myopathy in a Han Chinese patient with a rare MYH11 mutation: A case report
12/2/2022 12:50:19 PM | Browse: 213 | Download: 547
2
Exome analysis for Cronkhite-Canada syndrome: A case report
8/16/2022 1:35:32 AM | Browse: 141 | Download: 410
3
Autosomal dominant osteopetrosis type II resulting from a de novo mutation in the CLCN7 gene: A case report
7/5/2022 1:22:29 AM | Browse: 155 | Download: 332
4
Genetic characteristics of a patient with multiple primary cancers: A case report
9/28/2021 10:00:17 AM | Browse: 292 | Download: 654
5
Alport syndrome combined with lupus nephritis in a Chinese family: A case report
6/11/2021 9:22:18 AM | Browse: 244 | Download: 384
6
Apert syndrome diagnosed by prenatal ultrasound combined with magnetic resonance image and whole exome sequencing: A case report
1/25/2021 10:52:18 AM | Browse: 268 | Download: 367
7
Unexpected metastasis of intraductal papillary neoplasm of the bile duct without an invasive component to the brain and lungs: A case report
1/16/2020 7:58:40 AM | Browse: 587 | Download: 763
8
Histologic features and genomic alterations of primary colorectal adenocarcinoma predict the growth patterns of liver metastasis
7/14/2019 11:25:18 AM | Browse: 648 | Download: 1368
9
Clinical applications of high-throughput genetic diagnosis in inherited retinal dystrophies: Present challenges and future directions
5/29/2015 8:53:00 AM | Browse: 1013 | Download: 1293
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