Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes
✍ Scribed by Sulman Basit; Ghazanfar Ali; Naveed Wasif; Muhammad Ansar; Wasim Ahmad
- Publisher
- Springer
- Year
- 2010
- Tongue
- English
- Weight
- 389 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
To isolate a putative tumor suppressor gene(+ we have constructed a physical map and a detailed deletion map of chromosome region 8p2 I .3-p22, where loss of heterozygosity (LOH) has been frequently seen in human hepatocellular carcinomas (HCC), colorectal cancers (CRC), and non-small cell lung canc
## Abstract Germ‐line mutations in the serine‐threonine kinase gene __STK11__ (__LKB1__) cause Peutz–Jeghers syndrome (PJS), a rare autosomal dominantly inherited disease, characterized by hamartomatous polyposis and mucocutaneous pigmentation. __STK11__ mutations only account for about half of PJS