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American Journal of Medical Genetics|February 1, 1991
Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytesP B Jacky, Y R Ahuja, K Anyane-Yeboa, et al.American Journal of Medical Genetics|March 2, 1999
Deletion of 1q in a patient with acrofacial dysostosisD J Waggoner, D J Ciske, S B Dowton, et al.American Journal of Medical Genetics|August 10, 1999
Partial monosomy of distal 10q: three new cases and a reviewD J Waggoner, C K Chow, S B Dowton, et al.Prenatal Diagnosis|November 1, 1988
Prenatal diagnosis, fetal pathology, and cytogenetic analysis of mosaic trisomy 14S W Cheung, P L Kolacki, M S Watson, et al.Journal of Biomolecular NMR|February 14, 1998
Automated 1H and 13C chemical shift prediction using the BioMagResBankD S Wishart, M S Watson, R F Boyko, et al.Skeletal Radiology|July 29, 1999
Heterogeneous signal in bone marrow on MRI of children's feet: a normal finding?C R Pal, A D Tasker, S J Ostlere, et al.The British Journal of General Practice : the Journal of the Royal College of General Practitioners|November 4, 1998
Workload implications of community psychiatric nurse employment by a general practice: a pilot studyJ Bruce, M S Watson, D Watson, et al.The Annals of Thoracic Surgery|September 1, 1995
Anomalous origin of the right pulmonary artery from the aorta and CATCH 22 syndromeM C Johnson, M S Watson, A W Strauss, et al.American Journal of Medical Genetics|December 4, 1995
Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocationA J Whelan, M S Watson, F D Porter, et al.American Journal of Medical Genetics|February 1, 1988
Congenital heart defect in a patient with deletion of chromosome 7qG E Tiller, M S Watson, L M Duncan, et al.Pageof 36