Showing results (221-230 of 340) with videos related to
Sort By:
Pageof 34
American Journal of Hematology|January 24, 2015
Genome-wide association study follow-up identifies cyclin A2 as a regulator of the transition through cytokinesis during terminal erythropoiesisLeif S Ludwig, Hyunjii Cho, Aoi Wakabayashi, et al.Human Molecular Genetics|August 1, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung diseaseT Attié, A Pelet, P Edery, et al.Human Molecular Genetics|June 1, 1996
Mutational scanning of large genes by extensive PCR multiplexing and two-dimensional electrophoresis: application to the RB1 geneN J Van Orsouw, D Li, P van der Vlies, et al.Biochemical and Biophysical Research Communications|May 9, 2000
Analysis of hABC1 gene 5' end: additional peptide sequence, promoter region, and four polymorphismsC R Pullinger, H Hakamata, P N Duchateau, et al.The American Journal of Cardiology|September 21, 2001
Effects of omapatrilat on hemodynamics and safety in patients with heart failureM Klapholz, I Thomas, C Eng, et al.Oncogene|December 7, 1995
RET activation by germline MEN2A and MEN2B mutationsM G Borrello, D P Smith, B Pasini, et al.Journal of Medical Genetics|December 1, 1998
Mutations of PTEN in patients with Bannayan-Riley-Ruvalcaba phenotypeM Longy, V Coulon, B Duboué, et al.Journal of Medical Genetics|June 1, 1994
Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?C Eng, V Murday, S Seal, et al.JAMA|October 11, 1995
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type IIH P Neumann, C Eng, L M Mulligan, et al.Journal of Medical Genetics|August 3, 2000
RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung diseaseS Borrego, A Ruiz, M E Saez, et al.Pageof 34