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MOLTENO C
SMART R
VILJOEN D
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Authors:
AGARWAL SS
PHADKE SR
FREDLUND V
VILJOEN D
BEIGHTON P
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GARDNER JC
GOLIATH R
VILJOEN D
SELLARS S
CORTOPASSI G
HUTCHIN T
GREENBERG J
BEIGHTON P
Citation: Jc. Gardner et al., FAMILIAL STREPTOMYCIN OTOTOXICITY IN A SOUTH-AFRICAN FAMILY - A MITOCHONDRIAL DISORDER, Journal of Medical Genetics, 34(11), 1997, pp. 904-906
Authors:
BALLO R
VILJOEN D
MACHADO M
KEENE D
HORTON W
FREDLUND V
JACOBS M
MARTELL R
BEIGHTON P
RAMESAR R
Citation: R. Ballo et al., MSELENI JOINT DISEASE - A MOLECULAR-GENETIC APPROACH TO DEFINING THE ETIOLOGY, South African medical journal, 86(8), 1996, pp. 956-958
Authors:
VILJOEN D
OOSTHUIZEN C
VANDERWESTHUIZEN S
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NICOLE S
BENHAMIDA C
BEIGHTON P
BAKOURI S
BELAL S
ROMERO N
VILJOEN D
PONSOT G
SAMMOUD A
WEISSENBACH J
FARDEAU M
HAMIDA MB
FONTAINE B
HENTATI F
Citation: S. Nicole et al., LOCALIZATION OF THE SCHWARTZ-JAMPEL SYNDROME (SJS) LOCUS TO CHROMOSOME 1P34-P36.1 BY HOMOZYGOSITY MAPPING, Human molecular genetics, 4(9), 1995, pp. 1633-1636
Citation: R. Ballo et al., DUCHENNE AND BECKER MUSCULAR-DYSTROPHY PREVALENCE IN SOUTH-AFRICA ANDMOLECULAR FINDINGS IN 128 PERSONS AFFECTED, South African medical journal, 84(8), 1994, pp. 494-497
Citation: D. Viljoen, MACRODACTYLY OF BOTH HANDS AND FOOT ASSOCIATED WITH CUTANEOUS HEMANGIOMAS - A CASE-REPORT WITH REVIEW OF THE LITERATURE, Annals of saudi medicine, 14(5), 1994, pp. 426-426
Citation: J. Gardner et D. Viljoen, APLASIA-CUTIS-CONGENITA WITH EPIBULBAR DERMOIDS - FURTHER EVIDENCE FOR SYNDROMIC IDENTITY OF THE OCULAR ECTODERMAL SYNDROME, American journal of medical genetics, 53(4), 1994, pp. 317-320
Authors:
WALLIS GA
SYKES B
BYERS PH
MATHEW CG
VILJOEN D
BEIGHTON P
Citation: Ga. Wallis et al., OSTEOGENESIS IMPERFECTA TYPE-III - MUTATIONS IN THE TYPE-I COLLAGEN STRUCTURAL GENES, COL1A1 AND COL1A2, ARE NOT NECESSARILY RESPONSIBLE, Journal of Medical Genetics, 30(6), 1993, pp. 492-496