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Epilepsia|September 6, 2012
How should we be searching for genes for common epilepsy? A critique and a prescriptionDavid A Greenberg, William C L StewartBiometrics|September 21, 2006
Improving estimates of genetic maps: a maximum likelihood approachWilliam C L Stewart, Elizabeth A ThompsonDevelopmental Biology|February 1, 1994
Stem cells from primordial germ cells can reenter the germ lineC L Stewart, I Gadi, H BhattHuman Mutation|October 8, 2020
FREQMAX provides an alternative approach for determining high-resolution allele frequency thresholds in carrier screeningRyan L Subaran, William C L StewartHeredity|June 2, 2016
A powerful test of independent assortment that determines genome-wide significance quickly and accuratelyW C L Stewart, V R HagerHuman Heredity|October 6, 2012
Obtaining accurate p values from a dense SNP linkage scanWilliam C L Stewart, Ryan L SubaranThe Biochemical Journal|June 15, 1979
Copper metabolism in mottled mouse mutants: distribution of 64Cu in brindled (Mobr) miceJ R Mann, J Camakaris, D M DanksThe Biochemical Journal|February 15, 1980
Copper metabolism in mottled mouse mutants. Defective placental transfer of 64Cu to foetal brindled (Mobr) miceJ R Mann, J Camakaris, D M DanksThe Biochemical Journal|June 15, 1979
Copper metabolism in mottled mouse mutants: copper concentrations in tissues during developmentJ Camakaris, J R Mann, D M DanksTrends in Cardiovascular Medicine|November 16, 2001
The A-type lamins: nuclear structural proteins as a focus for muscular dystrophy and cardiovascular diseasesL C Mounkes, B Burke, C L StewartPageof 26