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Whole‐exome sequencing of nevoid basal cell carcinoma syndrome families and review of Human Gene Mutation Database PTCH1 mutation data.
- Published in:
- Molecular Genetics & Genomic Medicine, 2018, v. 6, n. 6, p. 1168, doi. 10.1002/mgg3.498
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- Publication type:
- Article
Variable Clinical Features in a Large Family With Diamond Blackfan Anemia Caused by a Pathogenic Missense Mutation in RPS19.
- Published in:
- 2022
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- Publication type:
- Case Study
Osteosarcoma: A Surveillance, Epidemiology, and End Results program‐based analysis from 1975 to 2017.
- Published in:
- Cancer (0008543X), 2022, v. 128, n. 11, p. 2107, doi. 10.1002/cncr.34163
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- Publication type:
- Article