M A Moreno-Pelayo - JoVE Visualize

Showing results (1-10 of 16) with videos related to

Pageof 2

Sort By:

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.

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.

Archivos De La Sociedad Espanola De Oftalmologia|July 10, 2021

Genetics and epidemiology of aniridia: Updated guidelines for genetic studyF Blanco-Kelly, M Tarilonte, M Villamar, et al.

Archivos De La Sociedad Espanola De Oftalmologia|November 27, 2021

Genetics and epidemiology of aniridia: Updated guidelines for genetic studyF Blanco-Kelly, M Tarilonte, M Villamar, 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.

Journal of Immunology (Baltimore, Md. : 1950)|October 6, 1998

C4d DNA sequences of two infrequent human allotypes (C4A13 and C4B12) and the presence of signal sequences enhancing recombinationN Martínez-Quiles, E Paz-Artal, M A Moreno-Pelayo, 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.

Acta Otorrinolaringologica Espanola|July 16, 2004

[Evaluation of a family with sensorineural hearing loss due to the Q829X mutation in the OTOF gene]J Gallo-Terán, R Megía López, C Morales-Angulo, et al.

Acta Otorrinolaringologica Espanola|October 14, 2006

[Auditory neuropathy due to the Q829X mutation in the gene encoding otoferlin (OTOF) in an infant screened for newborn hearing impairment]J Gallo-Terán, C Morales-Angulo, N Sánchez, et al.

Acta Otorrinolaringologica Espanola|October 6, 2004

[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity]J Gallo-Terán, B Arellano, C Morales-Angulo, et al.

Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:

Pageof 2

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.

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.

Archivos De La Sociedad Espanola De Oftalmologia|July 10, 2021

Genetics and epidemiology of aniridia: Updated guidelines for genetic studyF Blanco-Kelly, M Tarilonte, M Villamar, et al.

Archivos De La Sociedad Espanola De Oftalmologia|November 27, 2021

Genetics and epidemiology of aniridia: Updated guidelines for genetic studyF Blanco-Kelly, M Tarilonte, M Villamar, 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.

Journal of Immunology (Baltimore, Md. : 1950)|October 6, 1998

C4d DNA sequences of two infrequent human allotypes (C4A13 and C4B12) and the presence of signal sequences enhancing recombinationN Martínez-Quiles, E Paz-Artal, M A Moreno-Pelayo, 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.

Acta Otorrinolaringologica Espanola|July 16, 2004

[Evaluation of a family with sensorineural hearing loss due to the Q829X mutation in the OTOF gene]J Gallo-Terán, R Megía López, C Morales-Angulo, et al.

Acta Otorrinolaringologica Espanola|October 14, 2006

[Auditory neuropathy due to the Q829X mutation in the gene encoding otoferlin (OTOF) in an infant screened for newborn hearing impairment]J Gallo-Terán, C Morales-Angulo, N Sánchez, et al.

Acta Otorrinolaringologica Espanola|October 6, 2004

[Prevalence of the A1555G mutation in the mitochondrial DNA in patients with cochlear or vestibular damage due to aminoglycoside-induced ototoxicity]J Gallo-Terán, B Arellano, C Morales-Angulo, et al.

Pageof 2