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P2X7 and NRAMP1/SLC11 A1 gene polymorphisms in Mexican mestizo patients with pulmonary tuberculosis

✍ Scribed by P. Niño-Moreno; D. Portales-Pérez; B. Hernández-Castro; L. Portales-Cervantes; V. Flores-Meraz; L. Baranda; A. Gómez-Gómez; V. Acuña-Alonzo; J. Granados; R. González-Amaro

Book ID
110090532
Publisher
John Wiley and Sons
Year
2007
Tongue
English
Weight
241 KB
Volume
148
Category
Article
ISSN
0009-9104

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✍ Roberto Mendoza-Londono; Catherine D. Kashork; Lisa G. Shaffer; Robert Krance; S 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 160 KB 👁 1 views

## Abstract Greig cephalopolysyndactyly (GCPS; OMIM 175700) is an autosomal dominant condition caused by mutations of the gene __GLI3__, located on 7p13. To date, several cases of deletions and/or translocations involving this locus have been reported in patients with GCPS. __GLI3__ is a transcript