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Cancer Genetics and Cytogenetics
|
October 1, 1983
Chromosome studies in two human brain tumors
J A Rey, M J Bello, J M de Campos, et al.
Human Genetics
|
October 11, 2008
Gene symbol: RPGR. Disease: Retinitis Pigmentosa
Ascensión Giménez, R Riveiro, M J Trujillo-Tiebas, et al.
Human Mutation
|
June 30, 2000
Three novel mutations (P215L, T289P, and 3811-2 A-->G) in the rhodopsin gene in autosomal dominant retinitis pigmentosa in Spanish families
M Martinez-Gimeno, M J Trujillo, I Lorda, et al.
Archivos De La Sociedad Espanola De Oftalmologia
|
January 11, 2001
[Retinitis pigmentosa, pattern dystrophy and fundus flavimaculatus not related to mutations in rhodopsine, peripherin/RDS and ROM-1 genes]
Benítez Del Castillo JM, M J Trujillo, Del Río T, et al.
Clinical Genetics
|
April 1, 1984
Cytogenetic and clinical findings in ten 45,X/46,XY patients
M C Ayuso, M C Ramos, M C Bello, et al.
Human Genetics
|
February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0540
E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG
|
October 6, 2001
Is it necessary to treat all patients with idiopathic pulmonary fibrosis?
A Xaubet, C Agustí, P Luburich, et al.
Clinical Genetics
|
March 12, 2014
Overview of Bardet-Biedl syndrome in Spain: identification of novel mutations in BBS1, BBS10 and BBS12 genes
M Álvarez-Satta, S Castro-Sánchez, I Pereiro, et al.
Journal of Medical Genetics
|
October 4, 2002
Novel homozygous mutation in the alpha subunit of the rod cGMP gated channel (CNGA1) in two Spanish sibs affected with autosomal recessive retinitis pigmentosa
E Paloma, A Martínez-Mir, B García-Sandoval, et al.
Human Genetics
|
February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hd0510
E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
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of 27
Search research articles
Search
Showing results (81-90 of 264) with videos related to
Sort By:
Page
of 27
Cancer Genetics and Cytogenetics
|
October 1, 1983
Chromosome studies in two human brain tumors
J A Rey, M J Bello, J M de Campos, et al.
Human Genetics
|
October 11, 2008
Gene symbol: RPGR. Disease: Retinitis Pigmentosa
Ascensión Giménez, R Riveiro, M J Trujillo-Tiebas, et al.
Human Mutation
|
June 30, 2000
Three novel mutations (P215L, T289P, and 3811-2 A-->G) in the rhodopsin gene in autosomal dominant retinitis pigmentosa in Spanish families
M Martinez-Gimeno, M J Trujillo, I Lorda, et al.
Archivos De La Sociedad Espanola De Oftalmologia
|
January 11, 2001
[Retinitis pigmentosa, pattern dystrophy and fundus flavimaculatus not related to mutations in rhodopsine, peripherin/RDS and ROM-1 genes]
Benítez Del Castillo JM, M J Trujillo, Del Río T, et al.
Clinical Genetics
|
April 1, 1984
Cytogenetic and clinical findings in ten 45,X/46,XY patients
M C Ayuso, M C Ramos, M C Bello, et al.
Human Genetics
|
February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hm0540
E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
Sarcoidosis, Vasculitis, and Diffuse Lung Diseases : Official Journal of WASOG
|
October 6, 2001
Is it necessary to treat all patients with idiopathic pulmonary fibrosis?
A Xaubet, C Agustí, P Luburich, et al.
Clinical Genetics
|
March 12, 2014
Overview of Bardet-Biedl syndrome in Spain: identification of novel mutations in BBS1, BBS10 and BBS12 genes
M Álvarez-Satta, S Castro-Sánchez, I Pereiro, et al.
Journal of Medical Genetics
|
October 4, 2002
Novel homozygous mutation in the alpha subunit of the rod cGMP gated channel (CNGA1) in two Spanish sibs affected with autosomal recessive retinitis pigmentosa
E Paloma, A Martínez-Mir, B García-Sandoval, et al.
Human Genetics
|
February 14, 2007
Gene symbol: CRB1. Disease: Leber congenital amaurosis. Accession #Hd0510
E Vallespin, D Cantalapiedra, M Garcia-Hoyos, et al.
Page
of 27