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X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeatsGenomic structure and identification of novel mutations in usherin, the gene responsible for Usher syndrome type IIaA radiation hybrid breakpoint map of the acute myeloid leukemia (AML) and limb-girdle muscular dystrophy 1A (LGMD1A) regions of chromosome 5q31 localizing 122 expressed sequencesDiverse prevalence of large deletions within the OA1 gene in ocular albinism type 1 patients from Europe and North AmericaRetinitis pigmentosa locus on 17q (RP17): fine localization to 17q22 and exclusion of the PDEG and TIMP2 genesMultiple epiphyseal dysplasia, ribbing type: a novel point mutation in the COMP gene in a South African familyA genomic portrait of haplotype diversity and signatures of selection in indigenous southern African populationsReport on the 6th African Society of Human Genetics (AfSHG) Meeting, March 12-15, 2009, Yaounde, CameroonReady to put metadata on the post-2015 development agenda? Linking data publications to responsible innovation and science diplomacy.Neuropsychological dysfunction in bipolar affective disorder: a critical opinion.Arrhythmogenic right ventricular cardiomyopathy type 6 (ARVC6): support for the locus assignment, narrowing of the critical region and mutation screening of three candidate genesTrends in suicidology: personality as an endophenotype for molecular genetic investigations.Genetic variation at selected SNPs in the leptin gene and association of alleles with markers of kidney disease in a Xhosa population of South Africa.GENETICS. The Human Variome ProjectHaplotype-based study of the association of alcohol and acetaldehyde-metabolising genes with alcohol dependence (with or without comorbid anxiety symptoms) in a Cape Mixed Ancestry population.Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa.Computational analysis of candidate disease genes and variants for salt-sensitive hypertension in indigenous Southern AfricansRecommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.Possible involvement of the circadian pathway in alcohol use disorder in a South African adolescent cohort.The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.A mutation in a splicing factor that causes retinitis pigmentosa has a transcriptome-wide effect on mRNA splicing.Research capacity. Enabling the genomic revolution in Africa.CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.Genetic heterogeneity of Usher syndrome: analysis of 151 families with Usher type I.Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome.Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.The BDNF p.Val66Met polymorphism, childhood trauma, and brain volumes in adolescents with alcohol abuseDetermining ancestry proportions in complex admixture scenarios in South Africa using a novel proxy ancestry selection method.How to catch all those mutations--the report of the third Human Variome Project Meeting, UNESCO Paris, May 2010.Association of variants at BCL11A and HBS1L-MYB with hemoglobin F and hospitalization rates among sickle cell patients in Cameroon.Fertility and apparent genetic anticipation in Lynch syndrome.The importance of G protein-coupled receptor kinase 4 (GRK4) in pathogenesis of salt sensitivity, salt sensitive hypertension and response to antihypertensive treatment.Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trialExploring researchers' experiences of working with a researcher-driven, population-specific community advisory board in a South African schizophrenia genomics studyGenetic variants implicated in personality: a review of the more promising candidates.Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma.Apolipoprotein E variants and cognition in healthy individuals: a critical opinion.Neurocognitive function as an endophenotype for genetic studies of bipolar affective disorder.PXR and CAR single nucleotide polymorphisms influence plasma efavirenz levels in South African HIV/AIDS patients.Toward colorectal cancer control in Africa
P50
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P50
description
hulumtues
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onderzoeker
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հետազոտող
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Raj Ramesar
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Raj Ramesar
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Rajkumar Sewcharan Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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Rajkumar Ramesar
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P1053
I-6941-2015
P106
P1153
35373926300
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P3829
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0000-0001-5688-1634