𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Is it hereditary?: 2. Types and characteristic patterns of hereditary disease

✍ Scribed by M. THRUSFIELD


Book ID
114873443
Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
597 KB
Volume
29
Category
Article
ISSN
0022-4510

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Duplication of part of chromosome 17 is
✍ P. J. Hallam; A. E. Harding; J. Berciano; D. F. Barker; Dr S. Malcolm πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 477 KB πŸ‘ 3 views

Hereditary motor and sensory neuropathy type I (HMSNI), also known as Charcot-Marie-Tooth disease type 1 (CMTl), has been shown to be genetically heterogeneous. A major gene maps to chromosome 17 (CMTlA). A set of loci, D17S122, D17S125, and D17S124, show tight linkage to the C M T l A locus, and a

IGF1 is a modifier of disease risk in he
✍ Stuart G. Reeves; Dominique Rich; Cliff J. Meldrum; Kim Colyvas; Grzegorz Kurzaw πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 French βš– 109 KB πŸ‘ 1 views

## Abstract Patients diagnosed with HNPCC harbouring a confirmed germline mutation in DNA mismatch repair (MMR) genes have an 80% lifetime risk of developing an epithelial malignancy. There is, however, considerable variation in the age of disease onset in these patients. Insulin‐like growth factor