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D Araque

Showing results (1-10 of 3) with videos related to

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Anales De Pediatria (Barcelona, Spain : 2003)|May 21, 2013
[Mosaic trisomy 13]F Cammarata-Scalisi, D Araque, M A Lacruz-Rengel, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 22, 2017
Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complexF Cammarata-Scalisi, C Vidales Moreno, F Stock, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 23, 2016
Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A geneF Cammarata-Scalisi, K Natsuga, E Toyonaga, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Anales De Pediatria (Barcelona, Spain : 2003)|May 21, 2013
[Mosaic trisomy 13]F Cammarata-Scalisi, D Araque, M A Lacruz-Rengel, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 22, 2017
Two novel mutations in the TSC2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complexF Cammarata-Scalisi, C Vidales Moreno, F Stock, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 23, 2016
Early severe pachyonychia congenita subtype PC-K6a with a novel mutation in the KRT6A geneF Cammarata-Scalisi, K Natsuga, E Toyonaga, et al.
Pageof 1