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CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis

โœ Scribed by Yu, J.; Chen, Z.; Ni, Y.; Li, Z.


Book ID
125500744
Publisher
Oxford University Press
Year
2011
Tongue
English
Weight
732 KB
Volume
27
Category
Article
ISSN
0268-1161

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A T3 allele in the CFTR gene exacerbates
โœ Antoine Disset; Carine Michot; Ann Harris; Emanuele Buratti; Mireille Claustres; ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 425 KB

## Communicated by Garry Cutting The different alleles at the (TG)m(T)n polymorphic loci at the 3 0 end of the human CFTR intron 8 determine the efficiency by which exon 9 is spliced. We identified a novel TG12T3 allele in a congenital bilateral absence of vas deferens (CBAVD) patient who carries