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Clinical Genetics|December 1, 1983
Prader-Willi syndrome associated with inversion of chromosome 15E J Winsor, J P WelchClinical Genetics|June 1, 1984
The use of structured scenarios in genetic counsellingJ R Arnold, E J WinsorAmerican Journal of Human Genetics|September 1, 1978
Genetic and demographic aspects of Nova Scotia Niemann-Pick disease (type D)E J Winsor, J P WelchCMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|December 1, 1986
Prevalence and prenatal diagnosis of neural tube defects in Nova Scotia in 1980-84E J Winsor, B S BrownPrenatal Diagnosis|December 1, 1989
Familial marker chromosome due to 3:1 disjunction of t(9;15) in a grandparentE J Winsor, M I Van AllenAmerican Journal of Medical Genetics|July 1, 1993
Moving satellites and unstable chromosome translocations: clinical and cytogenetic implicationsS A Farrell, E J Winsor, V D MarkovicClinical Genetics|February 11, 2000
Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22)S Arab, D Chitayat, H A Gardner, et al.Cytogenetics and Cell Genetics|January 1, 1978
Meiotic studies in mice carrying the sex reversal (Sxr) factorE J Winsor, M A Ferguson-Smith, J G ShireAmerican Journal of Obstetrics and Gynecology|October 1, 1996
The role of fetal karyotyping from unconventional sourcesT G Teoh, G Ryan, J Johnson, et al.Child Abuse & Neglect|May 13, 1999
Predicting child maltreatment in the first 4 years of life from characteristics assessed in the neonatal periodJ B Kotch, D C Browne, V Dufort, et al.Pageof 4