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G Padberg

Showing results (11-20 of 16) with videos related to

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The British Journal of Dermatology|March 1, 1986
Neurological complications in patients with cutaneous T-cell lymphomaH J Sentis, G Padberg, O J Buruma, et al.
Arzneimittel-Forschung|January 1, 1977
[Toxicologic study on the antihypertensive agent urapidil]J König, E D Meier-Dörzenbach, H G Menge, et al.
Cancer|February 15, 1993
The prognosis of patients with stage III melanoma. Prospective long-term study of 286 patients of the Fachklinik HornheideH Drepper, B Biess, B Hofherr, et al.
American Journal of Human Genetics|January 1, 1995
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesM Zatz, S K Marie, M R Passos-Bueno, et al.
Oncogene|January 23, 1997
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regionsF Kerangueven, F Eisinger, T Noguchi, et al.
Journal of the Neurological Sciences|September 1, 1984
Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophyG Padberg, A W Eriksson, W S Volkers, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
The British Journal of Dermatology|March 1, 1986
Neurological complications in patients with cutaneous T-cell lymphomaH J Sentis, G Padberg, O J Buruma, et al.
Arzneimittel-Forschung|January 1, 1977
[Toxicologic study on the antihypertensive agent urapidil]J König, E D Meier-Dörzenbach, H G Menge, et al.
Cancer|February 15, 1993
The prognosis of patients with stage III melanoma. Prospective long-term study of 286 patients of the Fachklinik HornheideH Drepper, B Biess, B Hofherr, et al.
American Journal of Human Genetics|January 1, 1995
High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy familiesM Zatz, S K Marie, M R Passos-Bueno, et al.
Oncogene|January 23, 1997
Loss of heterozygosity in human breast carcinomas in the ataxia telangiectasia, Cowden disease and BRCA1 gene regionsF Kerangueven, F Eisinger, T Noguchi, et al.
Journal of the Neurological Sciences|September 1, 1984
Linkage studies in autosomal dominant facioscapulohumeral muscular dystrophyG Padberg, A W Eriksson, W S Volkers, et al.
Pageof 2