Winsor E - Search Results

1

Technical factors in early amniocentesis predict adverse outcome. Results of the Canadian Early (EA) versus Mid-trimester (MA) Amniocentesis Trial.

Johnson JM, Wilson RD, Singer J, Winsor E, Harman C, Armson BA, Benzie R, Dansereau J, Ho MF, Mohide P, Natale R, Okun N. Johnson JM, et al. Among authors: winsor e. Prenat Diagn. 1999 Aug;19(8):732-8. doi: 10.1002/(sici)1097-0223(199908)19:8<732::aid-pd624>3.0.co;2-n. Prenat Diagn. 1999. PMID: 10451517 Clinical Trial.

2

Cytogenetic aspects of the Canadian early and mid-trimester amniotic fluid trial (CEMAT).

Winsor EJ, Tomkins DJ, Kalousek D, Farrell S, Wyatt P, Fan YS, Carter R, Wang H, Dallaire L, Eydoux P, Welch JP, Dawson A, Lin JC, Singer J, Johnson J, Wilson RD. Winsor EJ, et al. Prenat Diagn. 1999 Jul;19(7):620-7. doi: 10.1002/(sici)1097-0223(199907)19:7<620::aid-pd599>3.0.co;2-e. Prenat Diagn. 1999. PMID: 10419609 Clinical Trial.

3

The early amniocentesis study: a randomized clinical trial of early amniocentesis versus midtrimester amniocentesis.

Johnson JM, Wilson RD, Winsor EJ, Singer J, Dansereau J, Kalousek DK. Johnson JM, et al. Among authors: winsor ej. Fetal Diagn Ther. 1996 Mar-Apr;11(2):85-93. doi: 10.1159/000264285. Fetal Diagn Ther. 1996. PMID: 8838763 Clinical Trial.

4

The early amniocentesis study: a randomized clinical trial of early amniocentesis and midtrimester amniocentesis. II. Evaluation of procedure details and neonatal congenital anomalies.

Wilson RD, Johnson J, Windrim R, Dansereau J, Singer J, Winsor EJ, Kalousek D. Wilson RD, et al. Among authors: winsor ej. Fetal Diagn Ther. 1997 Mar-Apr;12(2):97-101. doi: 10.1159/000264440. Fetal Diagn Ther. 1997. PMID: 9218950 Clinical Trial.

5

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

Okun N, Summers AM, Hoffman B, Huang T, Winsor E, Chitayat D, Staines A, Johnson JA. Okun N, et al. Among authors: winsor e. Prenat Diagn. 2008 Nov;28(11):987-92. doi: 10.1002/pd.2084. Prenat Diagn. 2008. PMID: 18925623

6

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

Lewinsky RM, Johnson JM, Lao TT, Winsor EJ, Cohen H. Lewinsky RM, et al. Among authors: winsor ej. Prenat Diagn. 1990 Sep;10(9):605-8. doi: 10.1002/pd.1970100909. Prenat Diagn. 1990. PMID: 2148373

7

The role of fetal karyotyping from unconventional sources.

Teoh TG, Ryan G, Johnson J, Winsor EJ. Teoh TG, et al. Among authors: winsor ej. Am J Obstet Gynecol. 1996 Oct;175(4 Pt 1):873-7. doi: 10.1016/s0002-9378(96)80016-0. Am J Obstet Gynecol. 1996. PMID: 8885739

8

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

Winsor EJ, Akoury H, Chitayat D, Steele L, Stockley TL. Winsor EJ, et al. Prenat Diagn. 2010 Aug;30(8):746-52. doi: 10.1002/pd.2530. Prenat Diagn. 2010. PMID: 20661888

9

Maternal cell contamination in uncultured amniotic fluid.

Winsor EJ, Silver MP, Theve R, Wright M, Ward BE. Winsor EJ, et al. Prenat Diagn. 1996 Jan;16(1):49-54. doi: 10.1002/(SICI)1097-0223(199601)16:1<49::AID-PD808>3.0.CO;2-U. Prenat Diagn. 1996. PMID: 8821852

10

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

Winsor EJ, Van Allen MI. Winsor EJ, et al. Prenat Diagn. 1989 Dec;9(12):851-5. doi: 10.1002/pd.1970091205. Prenat Diagn. 1989. PMID: 2626410

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