E. Winsor

J. Smallhorn, D. Chitayat, L. Hornberger, 2009, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The distribution of height and weight, and the influence of socio-economic factors, in a sample of eastern Canadian urban school children.

E. Winsor, J. Welch, S. Mackintosh, 1971 .

Genetics of childhood spinal muscular atrophy.

M. W. Thompson, T. Reed, E. Winsor, 1971, Journal of medical genetics.

Isodicentric Yp: prenatal diagnosis and outcome in 12 cases

B. Mcgillivray, D. Chitayat, H. Bruyèrè, 2006, Prenatal diagnosis.

Banding patterns in human chromosomes: production by proteolytic enzymes.

E. Winsor, J. Welch, C. L. Lee, 1972, The Journal of heredity.

The 11q;22q translocation: A collaborative study of 20 new cases and analysis of 110 families

A. Robinson, Y. Fukushima, N. Niikawa, 2004, Human Genetics.

Section 3: Prenatal screening and diagnosis of open neural tube defects

M. Ferguson-Smith, N. Wald, J. Haddow, 1981 .

Functional disomy of Xp: Prenatal findings and postnatal outcome

D. Chitayat, G. Seaward, E. Winsor, 2005, American journal of medical genetics. Part A.

Success Rate for Culture of Fetal Postmortem Tissue Is Dependent on the Method of Pregnancy Termination

D. Chitayat, G. Ryan, R. Windrim, 2005, Fetal Diagnosis and Therapy.

Tetrasomy 9p Mosaicism Associated with a Normal Phenotype

D. Chitayat, F. Mcauliffe, E. Winsor, 2005, Fetal Diagnosis and Therapy.

Inverted duplication of the distal short arm of chromosome 3 associated with lobar holoprosencephaly and lumbosacral meningomyelocele.

D. Ledbetter, D. Chitayat, A. Toi, 2000, American journal of medical genetics.

Moving satellites and unstable chromosome translocations: clinical and cytogenetic implications.

V. Markovic, S. Farrell, E. Winsor, 1993, American journal of medical genetics.

Meiotic studies in mice carrying the sex reversal (Sxr) factor.

M. Ferguson-Smith, J. Shire, E. Winsor, 1978, Cytogenetics and cell genetics.

Prospective validation of quantitative fluorescent polymerase chain reaction for rapid detection of common aneuploidies

D. Chitayat, D. Allingham-Hawkins, V. Cirigliano, 2011, Genetics in Medicine.

Randomized controlled trial of misoprostol for second-trimester pregnancy termination associated with fetal malformation.

T. Einarson, D. Chitayat, A. Willan, 2004, American journal of obstetrics and gynecology.

Trisomy 4 in a fetus with cyclopia and other anomalies.

A. Toi, K. Fong, M. V. Van Allen, 1993, American journal of medical genetics.

Human Chromosome 7: DNA Sequence and Biology

Junjun Zhang, Nazneen Rahman, Alexander K. Hudek, 2003, Science.

Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7.

M. Ferguson-Smith, C. Palmer, P. M. Ellis, 1978, Cytogenetics and cell genetics.

Prevalence and prenatal diagnosis of neural tube defects in Nova Scotia in 1980-84.

E. Winsor, B. S. Brown, 1986, CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne.

The role of fetal karyotyping from unconventional sources.

T. Teoh, G. Ryan, J. Johnson, 1996, American journal of obstetrics and gynecology.

Prenatal diagnosis and fetopathological findings in five fetuses with trisomy 9.

D. Chitayat, K. Hodgkinson, D. Kalousek, 1995, American journal of medical genetics.

Euchromatic 9q13-q21 duplication variants are tandem segmental amplifications of sequence reciprocal to 9q13-q21 deletions

S. Scherer, C. Marshall, C. Fahey, 2011, Journal of Medical Genetics.

Risk of false‐positive prenatal diagnosis using interphase FISH testing: hybridization of alpha‐satellite X probe to chromosome 19

S. Dyack, E. Winsor, Greg Ryan, 1999, Prenatal diagnosis.

Fetal gastroschisis associated with monosomy 22 mosaicism and absent cerebral diastolic flow

T. Lao, E. Winsor, J. Johnson, 1990, Prenatal diagnosis.

Familial marker chromosome due to 3:1 Disjunction of t(9;15) in a grandparent

M. V. Van Allen, E. Winsor, 1989, Prenatal diagnosis.

Prevalence of major mental retardation and associated disabilities in the Canadian Maritime Provinces.

J. B. Garner, E. Winsor, P. McQueen, 1987, American journal of mental deficiency.

Prospective experience with integrated prenatal screening and first trimester combined screening for trisomy 21 in a large Canadian urban center

Tianhua Huang, B. Hoffman, N. Okun, 2008, Prenatal diagnosis.

Winsor , Murphy , Thompson , and Reed

M. W. Thompson, T. Reed, E. Winsor, 2006 .

Proteomics Analysis of Human Amniotic Fluid *S

E. Diamandis, Eleftherios P Diamandis, Chan-Kyung J Cho, 2007, Molecular & Cellular Proteomics.

Prenatal detection of microtia by MRI in a fetus with trisomy 22

W. Halliday, D. Chitayat, A. Toi, 2006, Pediatric Radiology.

Assessment of the thymus at echocardiography in fetuses at risk for 22q11.2 deletion

J. Smallhorn, D. Chitayat, L. Hornberger, 2003, Prenatal diagnosis.

MATERNAL CELL CONTAMINATION IN UNCULTURED AMNIOTIC FLUID

B. Ward, E. Winsor, R. Theve, 1996, Prenatal diagnosis.

Deceased co‐twin as a cause of false positive amniotic fluid AFP and AChE

E. R. Luther, E. Winsor, J. Welch, 1987, Prenatal diagnosis.

The role of molecular microsatellite identity testing to detect sampling errors in prenatal diagnosis

D. Chitayat, E. Winsor, L. Steele, 2010, Prenatal diagnosis.

Prenatal ultrasound findings of lissencephaly associated with Miller–Dieker syndrome and comparison with pre‐ and postnatal magnetic resonance imaging

D. Chitayat, A. Toi, S. Blaser, 2004, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Huntington's chorea in Nova Scotia.

E. Winsor, J. Welch, 1973, The Nova Scotia medical bulletin.