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European Journal of Human Genetics : EJHG|January 1, 1996
Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigreeG Matthijs, S Claes, B Longo-Mbenza, et al.
Cytogenetics and Cell Genetics|January 1, 1995
A physical map of the region spanning the chromosome 12 translocation breakpoint in a mesothelioma with a t(X;12)(q22;p13)J Aerssens, C Guo, J Vermeesch, et al.
Cancer Research|February 15, 1997
Fusion of ETV6 to MDS1/EVI1 as a result of t(3;12)(q26;p13) in myeloproliferative disordersP Peeters, I Wlodarska, M Baens, et al.
Genomics|September 1, 1995
A radiation hybrid map with 60 loci covering the entire short arm of chromosome 12P Raeymaekers, K Van Zand, L Jun, et al.
Development (Cambridge, England)|November 1, 1993
Spatial and temporal changes in the expression of fibroglycan (syndecan-2) during mouse embryonic developmentG David, X M Bai, B Van der Schueren, et al.
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