Farrell SA - Search Results

1

Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.

Bruyère H, Speevak MD, Winsor EJ, de Fréminville B, Farrell SA, McGowan-Jordan J, McGillivray B, Chitayat D, McFadden D, Adouard V, Terespolsky D, Prieur F, Pantzar T, Hrynchak M. Bruyère H, et al. Among authors: farrell sa. Prenat Diagn. 2006 Apr;26(4):324-9. doi: 10.1002/pd.1406. Prenat Diagn. 2006. PMID: 16521154 Review.

2

An algorithm for the prenatal detection of chromosome anomalies by QF-PCR and G-banded analysis.

Speevak MD, Dolling J, Terespolsky D, Blumenthal A, Farrell SA. Speevak MD, et al. Among authors: farrell sa. Prenat Diagn. 2008 Dec;28(13):1221-6. doi: 10.1002/pd.2159. Prenat Diagn. 2008. PMID: 19039827

3

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.

4

Recombinant Down syndrome: a case report and literature review.

Lazzaro SJ, Speevak MD, Farrell SA. Lazzaro SJ, et al. Among authors: farrell sa. Clin Genet. 2001 Feb;59(2):128-30. doi: 10.1034/j.1399-0004.2001.590211.x. Clin Genet. 2001. PMID: 11260215 Review.

5

Molecular characterization of an inherited ring (19) demonstrating ring opening.

Speevak MD, Smart C, Unwin L, Bell M, Farrell SA. Speevak MD, et al. Among authors: farrell sa. Am J Med Genet A. 2003 Aug 30;121A(2):141-5. doi: 10.1002/ajmg.a.20184. Am J Med Genet A. 2003. PMID: 12910493

6

Non-syndromic language delay in a child with disruption in the Protocadherin11X/Y gene pair.

Speevak MD, Farrell SA. Speevak MD, et al. Among authors: farrell sa. Am J Med Genet B Neuropsychiatr Genet. 2011 Jun;156B(4):484-9. doi: 10.1002/ajmg.b.31186. Epub 2011 Apr 7. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21480486

7

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

Farrell SA, Winsor EJ, Markovic VD. Farrell SA, et al. Am J Med Genet. 1993 Jul 1;46(6):715-20. doi: 10.1002/ajmg.1320460624. Am J Med Genet. 1993. PMID: 8362916 Review.

8

Molecular and cytogenetic characterization of a prenatally ascertained de novo (X;Y) translocation.

Speevak M, Farrell SA, Chadwick D. Speevak M, et al. Among authors: farrell sa. Am J Med Genet. 2001 Jan 1;98(1):107-8. Am J Med Genet. 2001. PMID: 11426448 Review. No abstract available.

9

Charcot-Marie-Tooth 1B caused by expansion of a familial myelin protein zero (MPZ) gene duplication.

Speevak MD, Farrell SA. Speevak MD, et al. Among authors: farrell sa. Eur J Med Genet. 2013 Oct;56(10):566-9. doi: 10.1016/j.ejmg.2013.06.004. Epub 2013 Jun 25. Eur J Med Genet. 2013. PMID: 23811036

10

Infantile lethal variant of Simpson-Golabi-Behmel syndrome associated with hydrops fetalis.

Terespolsky D, Farrell SA, Siegel-Bartelt J, Weksberg R. Terespolsky D, et al. Among authors: farrell sa. Am J Med Genet. 1995 Nov 20;59(3):329-33. doi: 10.1002/ajmg.1320590310. Am J Med Genet. 1995. PMID: 8599356

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