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Author: Ballo, Robea

  • Author: Goldblatt, Jack
  • Author: Hayden, Michael Reuben
  • Author: Roberts, Tina Sharon
  • Author: Van Greunen, Francois
  • Author: Wallis, Colin E
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    An investigation into the molecular basis of familial forms of osteoarthropathy in South Africa
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    Duchenne muscular dystrophy in South Africa : molecular aspects

Author: Chetty, Manogari

  • Author: Goldblatt, Jack
  • Author: Hayden, Michael Reuben
  • Author: Roberts, Tina Sharon
  • Author: Van Greunen, Francois
  • Author: Wallis, Colin E
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    Dental implications of inherited connective tissue disorders in South Africa

Similar Items: Huntington’s chorea in South Africa

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    A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa
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    Molecular investigation of the trinucleotide repeats within the Huntington disease gene in Southern Africa
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    Predictive testing and clinical genetic counselling services for Huntington disease in the Western Cape : an evaluation over eleven years
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    The role of a genetic counsellor in a support group for Huntington disease
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    The molecular investigation of Stargardt disease in South Africa
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    Gaucer Disease in the Ashkenazi-Jewish Community of South Africa
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    The molecular genetic investigation of bipolar disorder in South Africa
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    An investigation into the molecular basis of familial forms of osteoarthropathy in South Africa
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    The molecular genetic and epidemiological investigation of colorectal cancer in South Africa
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    The experience of individuals with Huntingtons disease in the Western Cape, South Africa
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    Identification of a suitable SNP for allele-specific silencing of the disease-causing gene in SCA1 patients in South Africa
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    A molecular approach to Huntington disease in Southern Africa
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    Investigation of the ethnic differences and genetics of salt sensivity and salt-sensitive hypertension in South Africa
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    Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study
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    Genetics of age-related macular degeneration and Stargardt disease in South African populations
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    The molecular genetics of bipolar affective disorder : South African populations, endophenotypes, and environmental influence
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    Towards identifying the ADRP gene in a large South African family with retinitis pigmentosa
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    Sudden unexpected death in infants: a forensic genetic investigation in a South African cohort
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    A molecular investigation of the novel gene underlying autosomal dominant retinitis pigmentosa in a South African family
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    RNAi based allele-specific silencing of the disease-causing gene in black South African patients with SCA7
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    Novel cell models for the study of spinocerebellar ataxia type 7 pathogenesis and therapy in a South African patient cohort
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    APOE, PCSK9, and CETP genetic variants as potential biomarkers of dyslipidaemia in black South Africans with Type 2 Diabetes Mellitus
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    A Genome-wide Association Study of Schizophrenia in the South African Xhosa and Generalizability of Polygenic Risk Score across African populations
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    Investigation of the genetic aetiology of Parkinson's disease in South Africa

Similar Items: Gaucer Disease in the Ashkenazi-Jewish Community of South Africa

  • Similar Items: Dental implications of inherited connective tissue disorders in South Africa
  • Similar Items: Microcomputer-assisted diagnosis of inherited disorders of the skeleton
  • Similar Items: An investigation into the molecular basis of familial forms of osteoarthropathy in So...
  • Similar Items: Genetic disorders on the island of Mauritius
  • Similar Items: Dental implications of genetic and congenital intellectual disabilities in Cape Town
  • Similar Items: Duchenne muscular dystrophy in South Africa : molecular aspects
  • View Record
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    The molecular investigation of Stargardt disease in South Africa
  • Quick Look
    A molecular investigation of Huntington disease; origins of the mutation and current prevalence in South Africa
  • Quick Look
    Identification of a suitable SNP for allele-specific silencing of the disease-causing gene in SCA1 patients in South Africa
  • Quick Look
    Molecular investigation of the trinucleotide repeats within the Huntington disease gene in Southern Africa
  • Quick Look
    Genetics of age-related macular degeneration and Stargardt disease in South African populations
  • Quick Look
    Collective Singing in the Jewish Shtetl
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    Investigation of the genetic aetiology of Parkinson's disease in South Africa
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    RNAi based allele-specific silencing of the disease-causing gene in black South African patients with SCA7
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    Genetic analysis of inherited retinal diseases in indigenous Southern African populations
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    Huntington’s chorea in South Africa
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    Sickle cell trait and targeted genomic variants in chronic kidney disease an African cohort
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    The molecular genetic investigation of bipolar disorder in South Africa
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    Study of genetic modifiers of fetal hemoglobin and mechanisms of hydroxyurea-induced γ-globin expression in sickle cell disease
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    Predictive testing and clinical genetic counselling services for Huntington disease in the Western Cape : an evaluation over eleven years
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    An investigation into the molecular basis of familial forms of osteoarthropathy in South Africa
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    The molecular genetic and epidemiological investigation of colorectal cancer in South Africa
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    Development of a SCA7 patient-derived lymphoblast cell model for testing RNAi knock-down of the disease-causing gene
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    Association of variants in APOL1, MYH9 and HMOX1 WITH micro-Albuminuria among Sickle Cell disease patients from Cameroon
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    Pharmacogenomics of sickle cell disease therapeutics: pain and drug metabolism associated gene variants and hydroxyurea-induced post-transcriptional expression of miRNAs
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    Zionism and Hindutva: A Comparative Analysis of Jewish and Hindu Nationalism
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    Investigation of the ethnic differences and genetics of salt sensivity and salt-sensitive hypertension in South Africa
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    Spinocerebellar ataxia type 7 in southern africa: an epidemiological, molecular and cellular study
  • Quick Look
    The molecular genetics of bipolar affective disorder : South African populations, endophenotypes, and environmental influence
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    Towards identifying the ADRP gene in a large South African family with retinitis pigmentosa

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