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South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|August 1, 1996
Mseleni joint disease--a molecular genetic approach to defining the aetiologyR Ballo, D Viljoen, M Machado, et al.
Human Molecular Genetics|August 1, 1995
An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17qS Bardien, N Ebenezer, J Greenberg, et al.
American Journal of Human Genetics|February 1, 1990
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2B Sykes, D Ogilvie, P Wordsworth, et al.
Journal of Medical Genetics|September 3, 2002
Identification of a locus for a form of spondyloepiphyseal dysplasia on chromosome 15q26.1: exclusion of aggrecan as a candidate geneS Eyre, P Roby, K Wolstencroft, et al.
Human Molecular Genetics|September 1, 1995
Localization of the Schwartz-Jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mappingS Nicole, C Ben Hamida, P Beighton, et al.
Alcoholism, Clinical and Experimental Research|June 8, 2001
Fetal alcohol syndrome: an international perspectiveK R Warren, F J Calhoun, P A May, et al.
Human Genetics|September 1, 1990
Delta F508 testing of the DNA bank of the Royal Manchester Children's HospitalM J Schwarz, M Super, C Wallis, et al.
American Journal of Medical Genetics|January 1, 1991
Pseudoxanthoma elasticum: similar autosomal recessive subtype in Belgian and Afrikaner familiesA De Paepe, D Viljoen, M Matton, et al.
Human Genetics|January 1, 1985
Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome)K E Davies, M G Mattei, J F Mattei, et al.
American Journal of Human Genetics|May 20, 1999
X-linked late-onset sensorineural deafness caused by a deletion involving OA1 and a novel gene containing WD-40 repeatsM T Bassi, R S Ramesar, B Caciotti, et al.
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