Showing results (101-110 of 254) with videos related to
Sort By:
Pageof 26
Nature Genetics|October 1, 1993
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndromeR Weksberg, D R Shen, Y L Fei, et al.Nucleic Acids Research|December 15, 1996
Designer DNA-binding drugs: the crystal structure of a meta-hydroxy analogue of Hoechst 33258 bound to d(CGCGAATTCGCG)2G R Clark, C J Squire, E J Gray, et al.The Journal of Biological Chemistry|February 3, 2009
Defining the potassium binding region in an apple terpene synthaseSol Green, Christopher J Squire, Niels J Nieuwenhuizen, et al.Nature|August 4, 1983
Somatic inactivation of genes on chromosome 13 is a common event in retinoblastomaR Godbout, T P Dryja, J Squire, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|July 1, 1993
Detection of MYCN gene amplification and deletions of chromosome 1p in neuroblastoma by in situ hybridization using routine histologic sectionsP K Leong, P Thorner, H Yeger, et al.Aviation, Space, and Environmental Medicine|May 17, 2005
Color vision tests for aviation: comparison of the anomaloscope and three lantern typesTheresa J Squire, Marisa Rodriguez-Carmona, Anthony D B Evans, et al.Blood|February 3, 1998
Cloning and characterization of the human homolog of mouse Jak2I Dalal, E Arpaia, H Dadi, et al.Pediatric Pathology & Laboratory Medicine : Journal of the Society for Pediatric Pathology, Affiliated with the International Paediatric Pathology Association|November 14, 1997
Heterogeneity of MYCN amplification in a child with stroma-rich neuroblastoma (ganglioneuroblastoma)A N Lorenzana, M Zielenska, P Thorner, et al.Cancer|April 15, 1994
MYCN gene amplification in rhabdomyosarcomaD Driman, P S Thorner, M L Greenberg, et al.Journal of Pediatric Hematology/Oncology|June 11, 1999
Familial Evans syndrome: a report of an affected sibshipA G McLeod, M Pai, R F Carter, et al.Pageof 26