Search research articles
Contact Us
Filters
Showing results (11-20 of 33) with videos related to
Page
of 4
Sort By:
Clinical Genetics
|
August 1, 1987
Heterogeneity of pseudoxanthoma elasticum: delineation of a new form?
D L Viljoen, F M Pope, P Beighton
Journal of Medical Genetics
|
October 1, 1983
Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?
D L Viljoen, S L Sellars, P Beighton
Prenatal Diagnosis
|
March 1, 1991
Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome
D L Viljoen, Z Jaquire, D L Woods
Pediatric Dermatology
|
February 1, 1988
Cutaneous manifestations of the Proteus syndrome
D L Viljoen, N Saxe, C Temple-Camp
American Journal of Medical Genetics
|
December 1, 1988
Partial trisomy 9--further delineation of the phenotype
R D Smart, D L Viljoen, B Fraser
Journal of Medical Genetics
|
June 1, 1991
Deletion of chromosome 13 in Moebius syndrome
J J Slee, R D Smart, D L Viljoen
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 2, 2016
Fetal alcohol spectrum disorders: Prevalence rates in South Africa
L Olivier, L M G Curfs, D L Viljoen
Pediatric Radiology
|
January 1, 1987
The Proteus syndrome: the magnetic resonance and radiological features
B J Cremin, D L Viljoen, S Wynchank, et al.
American Journal of Medical Genetics
|
March 1, 1988
Polyostotic fibrous dysplasia with cranial hyperostosis: new entity or most severe form of polyostotic fibrous dysplasia?
D L Viljoen, G A Versfeld, W Losken, et al.
American Journal of Medical Genetics
|
May 1, 1987
Proteus syndrome in southern Africa: natural history and clinical manifestations in six individuals
D L Viljoen, M M Nelson, G de Jong, et al.
Page
of 4
Search research articles
Search
Showing results (11-20 of 33) with videos related to
Sort By:
Page
of 4
Clinical Genetics
|
August 1, 1987
Heterogeneity of pseudoxanthoma elasticum: delineation of a new form?
D L Viljoen, F M Pope, P Beighton
Journal of Medical Genetics
|
October 1, 1983
Familial aggregation of streptomycin ototoxicity: autosomal dominant inheritance?
D L Viljoen, S L Sellars, P Beighton
Prenatal Diagnosis
|
March 1, 1991
Prenatal diagnosis in autosomal dominant Beckwith-Wiedemann syndrome
D L Viljoen, Z Jaquire, D L Woods
Pediatric Dermatology
|
February 1, 1988
Cutaneous manifestations of the Proteus syndrome
D L Viljoen, N Saxe, C Temple-Camp
American Journal of Medical Genetics
|
December 1, 1988
Partial trisomy 9--further delineation of the phenotype
R D Smart, D L Viljoen, B Fraser
Journal of Medical Genetics
|
June 1, 1991
Deletion of chromosome 13 in Moebius syndrome
J J Slee, R D Smart, D L Viljoen
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde
|
June 2, 2016
Fetal alcohol spectrum disorders: Prevalence rates in South Africa
L Olivier, L M G Curfs, D L Viljoen
Pediatric Radiology
|
January 1, 1987
The Proteus syndrome: the magnetic resonance and radiological features
B J Cremin, D L Viljoen, S Wynchank, et al.
American Journal of Medical Genetics
|
March 1, 1988
Polyostotic fibrous dysplasia with cranial hyperostosis: new entity or most severe form of polyostotic fibrous dysplasia?
D L Viljoen, G A Versfeld, W Losken, et al.
American Journal of Medical Genetics
|
May 1, 1987
Proteus syndrome in southern Africa: natural history and clinical manifestations in six individuals
D L Viljoen, M M Nelson, G de Jong, et al.
Page
of 4