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Showing results (51-60 of 54) with videos related to

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Journal of Medical Genetics|February 9, 2007
New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophyD Marchant, K Yu, K Bigot, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 23, 2000
Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticumB Struk, L Cai, S Zäch, et al.
Molecular Vision|January 5, 1999
Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin geneG K Klintworth, J R Sommer, G Obrian, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|May 4, 2016
Abstracts from the 8th Annual Meeting of the Scientific Association of Swiss Radiation Oncology (SASRO)A S Allal, C Ares, P Dulguerov, et al.
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Showing results (51-60 of 54) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 54 results.
Journal of Medical Genetics|February 9, 2007
New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophyD Marchant, K Yu, K Bigot, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 23, 2000
Mutations of the gene encoding the transmembrane transporter protein ABC-C6 cause pseudoxanthoma elasticumB Struk, L Cai, S Zäch, et al.
Molecular Vision|January 5, 1999
Familial subepithelial corneal amyloidosis (gelatinous drop-like corneal dystrophy): exclusion of linkage to lactoferrin geneG K Klintworth, J R Sommer, G Obrian, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|May 4, 2016
Abstracts from the 8th Annual Meeting of the Scientific Association of Swiss Radiation Oncology (SASRO)A S Allal, C Ares, P Dulguerov, et al.
Pageof 6