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Clinical Genetics|May 1, 1986
Prometaphase chromosome analysis as a routine diagnostic techniqueI C Barnes, E L MaltbyJournal of Medical Genetics|April 1, 1984
Familial pericentric inversion (13) detected by antenatal diagnosisE L MaltbyJournal of Medical Genetics|May 1, 1987
Folate sensitive site at 10q23 and its expression as a deletionE L Maltby, S HigginsJournal of Medical Genetics|March 1, 1993
A case of deletion 14(q22.1-->q22.3) associated with anophthalmia and pituitary abnormalitiesJ Elliott, E L Maltby, B ReynoldsNeurology|July 1, 1997
Xp21 muscular dystrophy due to X chromosome inversionP S Baxter, E L Maltby, O QuarrellJournal of Neurology, Neurosurgery, and Psychiatry|April 1, 1986
Inherited multiple meningiomas: a clinical, pathological and cytogenetic study of an affected familyR D Battersby, J W Ironside, E L MaltbyCancer Genetics and Cytogenetics|April 1, 1988
Cytogenetic studies in 50 meningiomasE L Maltby, J W Ironside, R D BattersbyClinica Chimica Acta; International Journal of Clinical Chemistry|December 10, 1999
Laboratory medicine in the United Kingdom: 1948-1998 and beyondC P Price, I C BarnesJournal of Clinical Pathology|June 25, 2005
HER2 amplification status in breast cancer: a comparison between immunohistochemical staining and fluorescence in situ hybridisation using manual and automated quantitative image analysis scoring techniquesC M Ellis, M J Dyson, T J Stephenson, et al.Journal of Medical Genetics|April 1, 1992
Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocationI D Young, J M Zuccollo, E L Maltby, et al.Pageof 3