Results 181 to 190 of about 2,525,884 (192)

Genotyping microarray (gene chip) for the ABCR (ABCA4) gene†

Human Mutation, 2003
R A Lewis, F P M Cremers, M Hawlina
exaly  

Further evidence of association of the ABCA4 gene with cleft lip/palate

European Journal of Oral Sciences, 2012
Ariadne Letra, José Mauro Granjeiro
exaly  

Gene symbol: ABCA4. Disease: Stargardt disease.

Human genetics, 2010
Susana, Maia-Lopes, M, Castelo-Branco, E, Silva, J, Aguirre-Lamban, R, Riveiro-Alvarez, M J, Trujillo-Tiebas, C, Ayuso   +6 more
openaire   +1 more source

Microarray-based mutation analysis of the ABCA4 (ABCR) gene in autosomal recessive cone–rod dystrophy and retinitis pigmentosa

European Journal of Human Genetics, 2004
Carel B Hoyng, Rando Allikmets, Frans P M Cremers   +2 more
exaly  

Phenotype/genotype correlation in a case series of Stargardt’s patients identifies novel mutations in the ABCA4 gene

Eye, 2013
Andrew J Lotery
exaly  

Spectrum of ABCA4 (ABCR) gene mutations in Spanish patients with autosomal recessive macular dystrophies

Human Mutation, 2001
Roser Gonzàlez i Duarte, Susana Balcells, Lluïsa Vilageliu   +2 more
exaly  

Bilateral choroidal neovascularization associated with bilateral ABCA4 gene mutation

European Journal of Ophthalmology, 2012
Maurizio Battaglia Parodi, Francesco Bandello   +1 more
exaly  

GENE THERAPIES FOR STARGARDT DISEASE (ABCA4)

2020
openaire   +3 more sources

Human gene mutations. Gene symbol: ABCA4. Disease: Stargardt disease.

Human genetics, 2008
Jana Aguirre, Lamban, R, Riveiro-Alvarez, D, Cantalapiedra, E, Vallespin, C, Villaverde, A, Avila-Fernandez, M A, Lopez-Martinez, M J, Trujillo-Tiebas, C, Ayuso   +8 more
openaire   +1 more source

Genetic and Clinical Analysis of ABCA4-Associated Disease in African American Patients

Human Mutation, 2014
Bo Yuan, Rando Allikmets, Jana Zernant
exaly