Found: 3
Select item for more details and to access through your institution.
Trio-Based Low-Pass Genome Sequencing Reveals Characteristics and Significance of Rare Copy Number Variants in Prenatal Diagnosis.
- Published in:
- Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.742325
- By:
- Publication type:
- Article
Mate-pair genome sequencing reveals structural variants for idiopathic male infertility.
- Published in:
- Human Genetics, 2023, v. 142, n. 3, p. 363, doi. 10.1007/s00439-022-02510-4
- By:
- Publication type:
- Article
Applying targeted next generation sequencing to dried blood spot specimens from suspicious cases identified by tandem mass spectrometry-based newborn screening.
- Published in:
- Journal of Pediatric Endocrinology & Metabolism, 2017, v. 30, n. 9, p. 979, doi. 10.1515/jpem-2017-0003
- By:
- Publication type:
- Article