Search Results

Construction of a high-density linkage map and QTL detection for growth traits in South African abalone (Haliotis midae).

• Authors : Tshilate TS; Department of Genetics, Stellenbosch University, Matieland, South Africa.; Ishengoma E

Subjects: Quantitative Trait Loci* ; Chromosome Mapping* ; Polymorphism, Single Nucleotide*

• Source: Animal genetics [Anim Genet] 2024 Oct; Vol. 55 (5), pp. 744-760. Date of Electronic Publication: 2024 Jun 30.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 8605704 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Genetic linkage between Huntington disease and the D4S10 locus in South African families: further evidence against non-allelic heterogeneity.

• Authors : Greenberg LJ; Department of Human Genetics, University of Cape Town Medical School, Observatory, South Africa.; Martell RW

Subjects: Chromosomes, Human, Pair 4* ; Genetic Linkage*; Huntington Disease/Huntington Disease/Huntington Disease/*genetics

• Source: Human genetics [Hum Genet] 1991 Oct; Vol. 87 (6), pp. 701-8.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print Cited Medium: Print ISSN: 0340-6717 (Print)

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New Biomarkers Study Findings Have Been Reported by Investigators at University of Stellenbosch [A High-density Genetic Linkage Map and Qtl Identification for Growth Traits In Dusky Kob ( Argyrosomus Japonicus )].

• Source: Health & Medicine Week. 2024, pages. 2643

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Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans.

• Authors : Xu B; Departments of Psychiatry, Physiology and Cellular Biophysics, and Neuroscience, Columbia University Medical Center, New York, NY 10032.; Woodroffe A

Subjects: Gene Dosage* ; Genetic Linkage* ; Genetic Variation*

• Source: Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2009 Sep 29; Vol. 106 (39), pp. 16746-51. Date of Electronic Publication: Publisher: National Academy of Sciences Country of Publication: United States NLM ID: 7505876 Publication Model: Print-Electronic Cited Medium: Internet

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Preliminary evidence for linkage to chromosome 1q31-32, 10q23.3, and 16p13.3 in a South African cohort with bipolar disorder.

• Authors : Savitz J; Division of Human Genetics, Institute of Infectious Disease and Molecular Medicine, University of Cape Town, Cape Town, South Africa. ; Cupido CL

Subjects: Chromosomes, Human, Pair 1* ; Chromosomes, Human, Pair 10* ; Chromosomes, Human, Pair 16*

• Source: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics [Am J Med Genet B Neuropsychiatr Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235742 Publication Model: Print Cited Medium: Print ISSN: 1552-4841

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A linkage and family-based association analysis of a potential neurocognitive endophenotype of bipolar disorder.

• Authors : Savitz J; Division of Human Genetics, Institute for Infectious Disease and Molecular Medicine, University of Cape Town, South Africa. ; van der Merwe L

Subjects: Family* ; Genetic Linkage* ; Phenotype*

• Source: Neuromolecular medicine [Neuromolecular Med] 2007; Vol. 9 (2), pp. 101-16.Publisher: Humana Press Country of Publication: United States NLM ID: 101135365 Publication Model: Print Cited Medium: Print ISSN: 1535-1084

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Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners.

• Authors : Simonic I; MRC Neurogenetics Research Initiative, Pretoria, South Africa.; Nyholt DR

Subjects: Chromosomes, Human, Pair 11* ; Chromosomes, Human, Pair 2* ; Chromosomes, Human, Pair 8*

• Source: American journal of medical genetics [Am J Med Genet] 2001 Mar 08; Vol. 105 (2), pp. 163-7.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print)

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X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

• Authors : Christianson AL; Department of Human Genetics and Developmental Biology, Faculty of Medicine, University of Pretoria, South Africa.; Stevenson RE

Subjects: Genetic Linkage* ; X Chromosome*; Abnormalities, Multiple/Abnormalities, Multiple/Abnormalities, Multiple/*genetics

• Source: Journal of medical genetics [J Med Genet] 1999 Oct; Vol. 36 (10), pp. 759-66.Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print Cited Medium: Print ISSN:

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No evidence for linkage of chromosome 22 markers to schizophrenia in southern African Bantu-speaking families.

• Authors : Riley B; Department of Biochemistry and Molecular Genetics, St. Mary's Hospital Medical School, Imperial College, London, UK.; Mogudi-Carter M

Subjects: Chromosomes, Human, Pair 22* ; Genetic Linkage*; Schizophrenia/Schizophrenia/Schizophrenia/*genetics

• Source: American journal of medical genetics [Am J Med Genet] 1996 Nov 22; Vol. 67 (6), pp. 515-22.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7708900 Publication Model: Print Cited Medium: Print ISSN: 0148-7299 (Print)

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Mapping of the variegate porphyria (VP) gene: contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32.

• Authors : Warnich L; Department of Genetics, University of Stellenbosch, South Africa.; Meissner PN

Subjects: Chromosomes, Human, Pair 14* ; Genetic Linkage*; DNA, Satellite/DNA, Satellite/DNA, Satellite/*genetics

• Source: Human genetics [Hum Genet] 1996 May; Vol. 97 (5), pp. 690-2.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print Cited Medium: Print ISSN: 0340-6717 (Print)

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