Winsor EJ - Search Results

1

Mosaicism for a small marker chromosome resulting from a familial Robertsonian translocation (21;22).

Arab S, Chitayat D, Gardner HA, Winsor EJ. Arab S, et al. Among authors: winsor ej. Clin Genet. 1999 Nov;56(5):362-6. doi: 10.1034/j.1399-0004.1999.560504.x. Clin Genet. 1999. PMID: 10668926

2

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

Fong KW, Ghai S, Toi A, Blaser S, Winsor EJ, Chitayat D. Fong KW, et al. Among authors: winsor ej. Ultrasound Obstet Gynecol. 2004 Dec;24(7):716-23. doi: 10.1002/uog.1777. Ultrasound Obstet Gynecol. 2004. PMID: 15586369 Free article.

3

Functional disomy of Xp: prenatal findings and postnatal outcome.

Kolomietz E, Godbole K, Winsor EJ, Stockley T, Seaward G, Chitayat D. Kolomietz E, et al. Among authors: winsor ej. Am J Med Genet A. 2005 May 1;134(4):393-8. doi: 10.1002/ajmg.a.30652. Am J Med Genet A. 2005. PMID: 15793841

4

Tetrasomy 9p mosaicism associated with a normal phenotype.

McAuliffe F, Winsor EJ, Chitayat D. McAuliffe F, et al. Among authors: winsor ej. Fetal Diagn Ther. 2005 May-Jun;20(3):219-22. doi: 10.1159/000083909. Fetal Diagn Ther. 2005. PMID: 15824502

5

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

Joseph-George AM, He Y, Marshall CR, Wong RC, MacDonald JR, Fahey CA, Chitayat D, Chun K, Ryan G, Summers AM, Winsor EJ, Scherer SW. Joseph-George AM, et al. Among authors: winsor ej. J Med Genet. 2011 May;48(5):317-22. doi: 10.1136/jmg.2010.085662. Epub 2011 Mar 23. J Med Genet. 2011. PMID: 21429932

6

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

Allingham-Hawkins DJ, Chitayat D, Cirigliano V, Summers A, Tokunaga J, Winsor E, Chun K. Allingham-Hawkins DJ, et al. Genet Med. 2011 Feb;13(2):140-7. doi: 10.1097/GIM.0b013e3182036763. Genet Med. 2011. PMID: 21233717 Free article.

7

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

Chitayat D, Hodgkinson K, Luke A, Winsor E, Rose T, Kalousek D. Chitayat D, et al. Am J Med Genet. 1995 Apr 10;56(3):247-51. doi: 10.1002/ajmg.1320560302. Am J Med Genet. 1995. PMID: 7778583 Review.

8

Prenatally diagnosed neural tube defects: ultrasound, chromosome, and autopsy or postnatal findings in 212 cases.

Kennedy D, Chitayat D, Winsor EJ, Silver M, Toi A. Kennedy D, et al. Among authors: winsor ej. Am J Med Genet. 1998 May 26;77(4):317-21. doi: 10.1002/(sici)1096-8628(19980526)77:4<317::aid-ajmg13>3.0.co;2-l. Am J Med Genet. 1998. PMID: 9600743

9

De novo 46,XX,t(6;7)(q27;q11;23) associated with severe cardiovascular manifestations characteristic of supravalvular aortic stenosis and Williams syndrome.

von Dadelszen P, Chitayat D, Winsor EJ, Cohen H, MacDonald C, Taylor G, Rose T, Hornberger LK. von Dadelszen P, et al. Among authors: winsor ej. Am J Med Genet. 2000 Feb 14;90(4):270-5. doi: 10.1002/(sici)1096-8628(20000214)90:4<270::aid-ajmg2>3.0.co;2-r. Am J Med Genet. 2000. PMID: 10710222

10

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

Kennedy D, Silver MM, Winsor EJ, Toi A, Provias J, Macha M, Precht K, Ledbetter DH, Chitayat D. Kennedy D, et al. Among authors: winsor ej. Am J Med Genet. 2000 Mar 20;91(3):167-70. Am J Med Genet. 2000. PMID: 10756335

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