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Showing results (101-110 of 106) with videos related to

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The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 29, 1998
The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and boneO Montonen, S Ezer, U K Saarialho-Kere, et al.
Neurology|September 1, 2006
Cerebroretinal microangiopathy with calcifications and cystsT Linnankivi, L Valanne, A Paetau, et al.
Journal of Medical Genetics|September 13, 2005
Increased risk of cancer in patients with fumarate hydratase germline mutationH J Lehtonen, M Kiuru, S K Ylisaukko-Oja, et al.
Molecular Cell|July 14, 1998
Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndromeM Kestilä, U Lenkkeri, M Männikkö, et al.
American Journal of Human Genetics|November 1, 1974
Pericentric inversions of human chromosomes 9 and 10A de la Chapelle, J Schröder, K Stenstrand, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 23, 2001
[CADASIL disease: a hereditary arterial disease leading to brain infarctions and dementia]H Kalimo, T Aho, K Amberla, et al.
Pageof 11

Showing results (101-110 of 106) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 106 results.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|April 29, 1998
The gene defective in anhidrotic ectodermal dysplasia is expressed in the developing epithelium, neuroectoderm, thymus, and boneO Montonen, S Ezer, U K Saarialho-Kere, et al.
Neurology|September 1, 2006
Cerebroretinal microangiopathy with calcifications and cystsT Linnankivi, L Valanne, A Paetau, et al.
Journal of Medical Genetics|September 13, 2005
Increased risk of cancer in patients with fumarate hydratase germline mutationH J Lehtonen, M Kiuru, S K Ylisaukko-Oja, et al.
Molecular Cell|July 14, 1998
Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndromeM Kestilä, U Lenkkeri, M Männikkö, et al.
American Journal of Human Genetics|November 1, 1974
Pericentric inversions of human chromosomes 9 and 10A de la Chapelle, J Schröder, K Stenstrand, et al.
Duodecim; Laaketieteellinen Aikakauskirja|November 23, 2001
[CADASIL disease: a hereditary arterial disease leading to brain infarctions and dementia]H Kalimo, T Aho, K Amberla, et al.
Pageof 11