## Communicated by Mark H. Paalman Mutations in the gene GJB2 encoding connexin 26 (Cx26), a gap junction protein, have been shown to be responsible for a majority of recessive nonsyndromic hereditary hearing impairment in children. Over 60 different mutations in Cx26 have been reported. To obviat
Screening breast cancer patients for ATM mutations and polymorphisms by using denaturing high-performance liquid chromatography
β Scribed by David P. Atencio; Christopher M. Iannuzzi; Sheryl Green; Richard G. Stock; Jonine L. Bernstein; Barry S. Rosenstein
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 125 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0893-6692
- DOI
- 10.1002/em.1072
No coin nor oath required. For personal study only.
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