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Journal of Medical Genetics|December 1, 1984
A rare heterochromatic variant of chromosome 4Z Docherty, S M Bowser-Riley
Prenatal Diagnosis|January 1, 1988
The use of gamma glutamyl transferase activity in amniotic fluid in the detection of fetal trisomy 21S R Jones, S E Evans
Cancer Genetics and Cytogenetics|April 1, 1988
Secondary leukemia with a translocation (8;21)?S V Davies, J A Murray, S M Bowser-Riley
Clinical Genetics|May 1, 1975
Chromosomal mosaicism in amniotic fluid cell culturesG R Sutherland, S M Bowser-Riley, A D Bain
British Journal of Obstetrics and Gynaecology|April 1, 1988
Amniotic fluid alpha-fetoprotein subfractions in fetal Trisomy 21 affected pregnanciesS R Jones, S E Evans, L Gillan
Human Genetics|May 1, 1987
Electron microscopic investigations of synaptonemal complexes in an infertile human male carrier of a pericentric inversion inv(1)(p32q42). Regular loop formation but defective synapsis including a possible interchromosomal effectJ Batanian, M A Hulten
Molecular Reproduction and Development|March 1, 1994
Sperm nuclear chromatin transformations in somatic cell-free extractsS Banerjee, M A Hulten
The Oncologist|May 10, 2000
VEGF receptor signaling in tumor angiogenesisG McMahon
Environmental Health Perspectives|December 1, 1994
The genetics of human cancer: implications for ecotoxicologyG McMahon
Inorganic Chemistry|October 16, 2001
Triimidosulfonic acid and organometallic triimidosulfonates: S(+)-N(-) versus S=N bondingB Walfort, A P Leedham, C A Russell, et al.
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