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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Juan Carlos Zenteno

Department of Genetics

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran

Mexico City

Mexico

[email]@salud.gob.mx

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Affiliations

Department of Genetics, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico. 2005 - 2006
Department of Genetics and the Research Unit, Institute of Ophthalmology Conde de Valenciana, Mexico City, Mexico. 2006

References

Expanding the mutational spectrum in TGFBI-linked corneal dystrophies: Identification of a novel and unusual mutation (Val113Ile) in a family with granular dystrophy. Zenteno, J.C., Ramirez-Miranda, A., Santacruz-Valdes, C., Suarez-Sanchez, R. Mol. Vis. (2006) [Pubmed]
Anophthalmia-esophageal atresia syndrome caused by an SOX2 gene deletion in monozygotic twin brothers with markedly discordant phenotypes. Zenteno, J.C., Perez-Cano, H.J., Aguinaga, M. Am. J. Med. Genet. A (2006) [Pubmed]
Isolated ectrodactyly caused by a heterozygous missense mutation in the transactivation domain of TP63. Zenteno, J.C., Berdón-Zapata, V., Kofman-Alfaro, S., Mutchinick, O.M. Am. J. Med. Genet. A (2005) [Pubmed]
CRYGD gene analysis in a family with autosomal dominant congenital cataract: evidence for molecular homogeneity and intrafamilial clinical heterogeneity in aculeiform cataract. Zenteno, J.C., Morales, M.E., Moran-Barroso, V., Sanchez-Navarro, A. Mol. Vis. (2005) [Pubmed]