Výsledky vyhledávání - "Viljoen, D L"

Prader-Willi syndrome in South African patients clinical and molecular diagnosis

Autor: Christianson, A. L., Viljoen, D. L., Winship, W. S., La Rey, M., Elizabeth van Rensburg

Publikováno v: South African Medical Journal; Vol 88, No 6 (1998); 711-714
Scopus-Elsevier

Study objective. To assess clinically South African patients with the putative diagnosis of Prader-Willi syndrome (PWS) and confirm this diagnosis by DNA/molecular analysis.Design. Prospective, nationally based, combined clinical and laboratory study

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b953220eb998b6e06eccb2d86f50fa8a
https://www.ajol.info/index.php/samj/article/view/149258

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Computerized electronic temperature control system for thermal efficiency during baking in food research.

Autor: Viljoen, D. L.¹ (AUTHOR), Muller, M.¹ (AUTHOR), De Swardt, J. B.² (AUTHOR), Sadie, A.³ (AUTHOR), Vosloo, M. C.¹ (AUTHOR)

Publikováno v: International Journal of Consumer Studies. Mar2001, Vol. 25 Issue 1, p30-42. 13p. 12 Charts.

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Microcephaly-cardiomyopathy: a new autosomal recessive phenotype?

Autor: Ingrid Winship, Viljoen, D. L., Leary, P. M., Moor, M. M.

Publikováno v: Scopus-Elsevier

A distinctive phenotype of severe microcephaly and self-limiting dilated cardiomyopathy has been observed in two sibs suggesting autosomal recessive inheritance. Mental retardation, delayed developmental milestones, and minor dysmorphism were additio

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::04776151dc5a7bd63470a9abffa2b9bf
https://europepmc.org/articles/PMC1015794/