Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome
Yobb, Twila M., Somerville, Martin J., Willatt, Lionel, Firth, Helen V., Harrison, Karen, MacKenzie, Jennifer, Gallo, Natasha, Morrow, Bernice E., Shaffer, Lisa G., Babcock, Melanie, Chernos, Judy, Bernier, Francois, Sprysak, Kathy, Christiansen, Jesse, Haase, Shelagh, Elyas, Basil, Lilley, Margaret, Bamforth, Steven, McDermid, Heather E.
Published in American journal of human genetics (01.05.2005)
Published in American journal of human genetics (01.05.2005)
Get full text
Journal Article
Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease
Christiansen, Jesse, Dyck, John D, Elyas, Basil G, Lilley, Margaret, Bamforth, J Stephen, Hicks, Mark, Sprysak, Kathleen A, Tomaszewski, Robert, Haase, Shelagh M, Vicen-Wyhony, Leanne M, Somerville, Martin J
Published in Circulation research (11.06.2004)
Published in Circulation research (11.06.2004)
Get full text
Journal Article
Toward optimal detection of the common prenatal aneuploidies by quantitative fluorescent-polymerase chain reaction: comparison of two commercial assays
Scott, Patrick, Podemski, Lynn, Baptista Wyatt, Kelly, Walker, Christine, Haase, Shelagh M, Elyas, Basil G, Sprysak, Kathleen A, Lilley, Margaret, Christian, Susan, Hicks, Mark, Somerville, Martin J, Hume, Stacey L
Published in Genetic testing and molecular biomarkers (01.08.2012)
Published in Genetic testing and molecular biomarkers (01.08.2012)
Get more information
Journal Article
Integration of combined heteroduplex/restriction fragment length polymorphism analysis on an electrophoresis microchip for the detection of hereditary haemochromatosis
FOOTZ, Tim, SOMERVILLE, Martin J, TOMASZEWSKI, Robert, ELYAS, Basil, BACKHOUSE, Christopher J
Published in Analyst (London) (01.01.2004)
Published in Analyst (London) (01.01.2004)
Get full text
Journal Article