Gene and Genome Sequencing: Interpreting Genetic Variation at the Nucleotide Level-Reference-Cited by-同舟云学术

Gene and Genome Sequencing: Interpreting Genetic Variation at the Nucleotide Level

Published:2017 Issue: Volume: Page:419-454
ISSN:
Container-title:Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis
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Author:

Wyandt Herman E.,Wilson Golder N.,Tonk Vijay S.

Publisher

Springer Singapore

Link

http://link.springer.com/content/pdf/10.1007/978-981-10-3035-2_11

Reference66 articles.

1. Hap Map Consortium (2010) Integrating common and rare genetic variation in diverse human populations. Nature 467:51–58. See the HapMap home page at http://hapmap.ncbi.nlm.nih.gov/

2. Macias VR et al (1992) Clasped thumb-mental retardation (MASA) syndrome: confirmation of linkage to Xq28. Am J Med Genet 43(408–414):1992

3. Online Mendelian Inheritance in Man. http://www.omim.org/ . Accessed 14 Jan 16

4. 1000 genomes: a deep catalogue of human variation. http://www.1000genomes.org/ . Accessed 12 Jan 16

5. Huisman THJ (1996) A syllabus of human hemoglobin variants. Pennsylvania State University. http://globin.cse.psu.edu/html/huisman/variants/ . Accessed 12 Jan 16

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