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UnknownCorrection: Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis.
Not available
S-EPMC4816403 | biostudies-literature
UnknownExome sequencing of index patients with retinal dystrophies as a tool for molecular diagnosis.
Not available
S-EPMC3683009 | biostudies-literature
UnknownPharmacogenetics of methylphenidate in childhood attention-deficit/hyperactivity disorder: long-term effects.
Not available
S-EPMC5583388 | biostudies-literature
UnknownNew CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report.
Not available
S-EPMC5219735 | biostudies-literature
UnknownMolecular analysis of ABCA4 and CRB1 genes in a Spanish family segregating both Stargardt disease and autosomal recessive retinitis pigmentosa.
Not available
S-EPMC2258218 | biostudies-literature
UnknownEarly noninvasive prenatal detection of a fetal CRB1 mutation causing Leber congenital amaurosis.
Not available
S-EPMC2493031 | biostudies-literature
UnknownGenotyping microarray: mutation screening in Spanish families with autosomal dominant retinitis pigmentosa.
Not available
S-EPMC3380913 | biostudies-literature
UnknownPartial paternal uniparental disomy (UPD) of chromosome 1 in a patient with Stargardt disease.
Not available
S-EPMC2553007 | biostudies-literature
UnknownAttention deficit hyperactivity disorder: genetic association study in a cohort of Spanish children.
Not available
S-EPMC4706690 | biostudies-literature
UnknownMethylation analysis by targeted bisulfite sequencing in large for gestational age (LGA) newborns: the LARGAN cohort.
Not available
S-EPMC10717641 | biostudies-literature
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