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J M Millán

Showing results (1-10 of 70) with videos related to

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Medicina Clinica|May 6, 1998
[Genetic research on Usher's syndrome in Spain]C Espinós, J M Millán
Medicina Clinica|January 15, 1994
[Molecular genetics of pigmentary retinopathy]J M Millán, C Nájera, M Beneyto
Neurologia (Barcelona, Spain)|March 1, 1993
[New magnetic resonance findings in the Meige syndrome]W Díaz Neira, M Lousa, J M Millán
The Journal of Investigative Dermatology|September 1, 1999
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg)F Martínez, J M Millán, C Orellana, et al.
Community Genetics|June 5, 2004
Epidemiology of Usher syndrome in Valencia and SpainC Espinós, J M Millán, M Beneyto, et al.
Genetic Epidemiology|January 1, 1995
Epidemiology of retinitis pigmentosa in the Valencian community (Spain)C Nájera, J M Millán, M Beneyto, et al.
Surgical Neurology|February 1, 1990
Cranial fasciitis of childhood with reactive periostitisM Mollejo, J M Millán, C Ballestin, et al.
Medicina Clinica|April 28, 1984
[Hemorrhagic cerebral infarct. Clinical characteristics and cranial computerized tomography]L Calandre, J A Molina, J M Millán, et al.
Actas Urologicas Espanolas|June 11, 2002
[Microsatellite analysis of the 3p13-p25 region in renal cell carcinoma in humans]M Aliaga, J M Millán Salvador, J F Jiménez Cruz
The Journal of Laryngology and Otology|December 29, 2000
Fatal cerebral venous sinus thrombosis as major complication of metastatic cervical mass: computed tomography and magnetic resonance findingsM F López-Peláez, J M Millán, J de Vergas
Pageof 7

Showing results (1-10 of 70) with videos related to

Sort By:
Pageof 7
Medicina Clinica|May 6, 1998
[Genetic research on Usher's syndrome in Spain]C Espinós, J M Millán
Medicina Clinica|January 15, 1994
[Molecular genetics of pigmentary retinopathy]J M Millán, C Nájera, M Beneyto
Neurologia (Barcelona, Spain)|March 1, 1993
[New magnetic resonance findings in the Meige syndrome]W Díaz Neira, M Lousa, J M Millán
The Journal of Investigative Dermatology|September 1, 1999
X-linked anhidrotic (hypohidrotic) ectodermal dysplasia caused by a novel mutation in EDA1 gene: 406T > G (Leu55Arg)F Martínez, J M Millán, C Orellana, et al.
Community Genetics|June 5, 2004
Epidemiology of Usher syndrome in Valencia and SpainC Espinós, J M Millán, M Beneyto, et al.
Genetic Epidemiology|January 1, 1995
Epidemiology of retinitis pigmentosa in the Valencian community (Spain)C Nájera, J M Millán, M Beneyto, et al.
Surgical Neurology|February 1, 1990
Cranial fasciitis of childhood with reactive periostitisM Mollejo, J M Millán, C Ballestin, et al.
Medicina Clinica|April 28, 1984
[Hemorrhagic cerebral infarct. Clinical characteristics and cranial computerized tomography]L Calandre, J A Molina, J M Millán, et al.
Actas Urologicas Espanolas|June 11, 2002
[Microsatellite analysis of the 3p13-p25 region in renal cell carcinoma in humans]M Aliaga, J M Millán Salvador, J F Jiménez Cruz
The Journal of Laryngology and Otology|December 29, 2000
Fatal cerebral venous sinus thrombosis as major complication of metastatic cervical mass: computed tomography and magnetic resonance findingsM F López-Peláez, J M Millán, J de Vergas
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