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Prenatal Diagnosis|September 1, 1990
Fetal gastroschisis associated with monosomy 22 mosaicism and absent cerebral diastolic flowR M Lewinsky, J M Johnson, T T Lao, et al.
American Journal of Mental Deficiency|March 1, 1987
Prevalence of major mental retardation and associated disabilities in the Canadian Maritime ProvincesP C McQueen, M W Spence, J B Garner, et al.
Developmental Medicine and Child Neurology|December 1, 1986
Causal origins of major mental handicap in the Canadian Maritime provincesP C McQueen, M W Spence, E J Winsor, et al.
Prenatal Diagnosis|September 1, 1987
Deceased co-twin as a cause of false positive amniotic fluid AFP and AChEE J Winsor, B S Brown, E R Luther, et al.
Prenatal Diagnosis|April 5, 2001
Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient managementW Cheong Leung, D Chitayat, G Seaward, et al.
Cytogenetics and Cell Genetics|January 1, 1978
Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7E J Winsor, C G Palmer, P M Ellis, et al.
Fetal Diagnosis and Therapy|March 1, 1997
The early amniocentesis study: a randomized clinical trial of early amniocentesis and midtrimester amniocentesis. II. Evaluation of procedure details and neonatal congenital anomaliesR D Wilson, J Johnson, R Windrim, et al.
Fetal Diagnosis and Therapy|March 1, 1996
The early amniocentesis study: a randomized clinical trial of early amniocentesis versus midtrimester amniocentesisJ M Johnson, R D Wilson, E J Winsor, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 27, 2025
The IL-18 receptor is expressed on murine small-intestinal enterochromaffin cells and executes a recovery program upon injuryNathaniel J Winsor, Derek K Tsang, Adrienne Ranger, et al.
American Journal of Medical Genetics|March 10, 2000
De novo 46,XX,t(6;7)(q27;q11;23) associated with severe cardiovascular manifestations characteristic of supravalvular aortic stenosis and Williams syndromeP von Dadelszen, D Chitayat, E J Winsor, et al.
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