I del Castillo - JoVE Visualize

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Acta Otorrinolaringologica Espanola|April 27, 1999

[Non-syndromic familial hearing impairment transmitted by mitochondrial inheritance]C Morales Angulo, I Del Castillo, M Sarduy, et al.

Clinical Genetics|January 8, 2008

Stickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genesL Olavarrieta, C Morales-Angulo, I del Castillo, et al.

Archives of Otolaryngology--Head & Neck Surgery|September 9, 2000

Sensorineural hearing loss and Mondini dysplasia caused by a deletion at locus DFN3B Arellano, R Ramírez Camacho, J R García Berrocal, et al.

Water Research|January 24, 2012

Self-bioremediation of cork-processing wastewaters by (chloro)phenol-degrading bacteria immobilised onto residual cork particlesI del Castillo, P Hernández, A Lafuente, et al.

Clinical and Experimental Rheumatology|August 15, 2002

Association analysis of genotypic frequencies of matrilin-1 gene in patients with osteoarthritisI Strusberg, A Sembaj, S Tabares, et al.

Genomics|August 1, 1993

Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndromeR Legouis, M Cohen-Salmon, I del Castillo, et al.

Parasitology|April 13, 2004

Remote sensing of intraperitoneal parasitism by the host's brain: regional changes of c-fos gene expression in the brain of feminized cysticercotic male miceJ Morales-Montor, I Arrieta, L I Del Castillo, et al.

Acta Otorrinolaringologica Espanola|January 24, 2006

[Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood onset]J Gallo-Terán, C Morales-Angulo, M Rodríguez-Ballesteros, et al.

Acta Otorrinolaringologica Espanola|February 15, 2003

[Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)]C Morales Angulo, J Gallo Terán, I del Castillo, et al.

Acta Otorrinolaringologica Espanola|January 18, 2003

[Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria]J Gallo-Terán, C Morales-Angulo, I del Castillo, et al.

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Showing results (11-20 of 36) with videos related to

Sort By:

Pageof 4

Acta Otorrinolaringologica Espanola|April 27, 1999

[Non-syndromic familial hearing impairment transmitted by mitochondrial inheritance]C Morales Angulo, I Del Castillo, M Sarduy, et al.

Clinical Genetics|January 8, 2008

Stickler and branchio-oto-renal syndromes in a patient with mutations in EYA1 and COL2A1 genesL Olavarrieta, C Morales-Angulo, I del Castillo, et al.

Archives of Otolaryngology--Head & Neck Surgery|September 9, 2000

Sensorineural hearing loss and Mondini dysplasia caused by a deletion at locus DFN3B Arellano, R Ramírez Camacho, J R García Berrocal, et al.

Water Research|January 24, 2012

Self-bioremediation of cork-processing wastewaters by (chloro)phenol-degrading bacteria immobilised onto residual cork particlesI del Castillo, P Hernández, A Lafuente, et al.

Clinical and Experimental Rheumatology|August 15, 2002

Association analysis of genotypic frequencies of matrilin-1 gene in patients with osteoarthritisI Strusberg, A Sembaj, S Tabares, et al.

Genomics|August 1, 1993

Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndromeR Legouis, M Cohen-Salmon, I del Castillo, et al.

Parasitology|April 13, 2004

Remote sensing of intraperitoneal parasitism by the host's brain: regional changes of c-fos gene expression in the brain of feminized cysticercotic male miceJ Morales-Montor, I Arrieta, L I Del Castillo, et al.

Acta Otorrinolaringologica Espanola|January 24, 2006

[Prevalence of the 35delG mutation in the GJB2 gene, del (GJB6-D13S1830) in the GJB6 gene, Q829X in the OTOF gene and A1555G in the mitochondrial 12S rRNA gene in subjects with non-syndromic sensorineural hearing impairment of congenital/childhood onset]J Gallo-Terán, C Morales-Angulo, M Rodríguez-Ballesteros, et al.

Acta Otorrinolaringologica Espanola|February 15, 2003

[Audiometric features of familial hearing impairment transmitted by mitochondrial inheritance (A1555G)]C Morales Angulo, J Gallo Terán, I del Castillo, et al.

Acta Otorrinolaringologica Espanola|January 18, 2003

[Incidence of A1555G mutations in the mitochondrial DNA and 35delG in the GJB2 gene (connexin-26) in families with late onset non-syndromic sensorineural hearing loss from Cantabria]J Gallo-Terán, C Morales-Angulo, I del Castillo, et al.

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