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Analysis of Human Genetic Linkage
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“Intriguingly, there are three instances of ASD cases with de novo deletions of 16p11.2 who also had an affected sibling without this deletion 157–159 along with similar observations for SV in 1q21.1 and 17p12. 158”
From Genetic architectures of psychiatric disorders: the emerging picture and its implications (2012) · cites this paper as [157]
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Metadata
- Authors
- Ott, J.
- Venue
- Johns Hopkins University Press eBooks
- Publisher
- Johns Hopkins University Press
- Published
- 1999
- OpenAlex
- W4319590830
- Cited by
- 754
- References
- 0
- Citations by year
- 2026: 2 · 2025: 3 · 2024: 3 · 2023: 9 · 2022: 6 · 2021: 11 · 2020: 15 · 2019: 8 · 2018: 12 · 2017: 22 · 2016: 15 · 2015: 14 · 2014: 20 · 2013: 18 · 2012: 25
- FWCI
- 38.33
- Type
- book
- Language
- en
- Open access
- closed
- Locations
- Johns Hopkins University Press eBooks (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Mapping and Diversity in Plants and Animals
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Forensic and Genetic Research
- Keywords
- linkage analysis, gene mapping, human genetics
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