Complex diseases are common genetic disorders showing familial aggregation but no typical Mendelian inheritance. Hirschsprung disease (HSCR), a developmental disorder characterized by the absence of enteric neurons in distal segments of the gut, shows a complex pattern of inheritance, with the RET p
โฆ LIBER โฆ
A common variant in the Von Willebrand factor gene is associated with multiple functional consequences
โ Scribed by Dhananjay Vaidya; Lisa R. Yanek; J. Enrique Herrera-Galeano; Rasika A. Mathias; Taryn F. Moy; Nauder Faraday; Lewis C. Becker;; Diane M. Becker
- Book ID
- 102697756
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 639 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0361-8609
No coin nor oath required. For personal study only.
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