A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene
Fonseca, D.J., Rojas, R.F., Vergara, J.I., Ríos, X., Uribe, C., Chávez, L., Velandia, F., Vargas, C.I., Restrepo, C.M., Laissue, P.
Published in British journal of dermatology (1951) (01.02.2013)
Published in British journal of dermatology (1951) (01.02.2013)
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Journal Article
A novel TGM1 mutation, leading to multiple splicing rearrangements, is associated with autosomal recessive congenital ichthyosis
Ortega-Recalde, O., Moreno, M. B., Vergara, J. I., Fonseca, D. J., Rojas, R. F., Mosquera, H., Medina, C. L., Restrepo, C. M., Laissue, P.
Published in Clinical and experimental dermatology (01.10.2015)
Published in Clinical and experimental dermatology (01.10.2015)
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Journal Article
Preserving privacy while reducing power consumption and information loss in LBS and participatory sensing applications
Vergara-Laurens, I. J., Labrador, M. A.
Published in 2011 IEEE GLOBECOM Workshops (GC Wkshps) (01.12.2011)
Published in 2011 IEEE GLOBECOM Workshops (GC Wkshps) (01.12.2011)
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Conference Proceeding
A severe familial phenotype of Ichthyosis Curth-Macklin caused by a novel mutation in the KRT1 gene
Fonseca, D J, Rojas, R F, Vergara, J I, Ríos, X, Uribe, C, Chávez, L, Velandia, F, Vargas, C I, Restrepo, C M, Laissue, P
Published in The British journal of dermatology (01.02.2013)
Published in The British journal of dermatology (01.02.2013)
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