Docherty Z - Search Results

1

Combined QF-PCR and MLPA molecular analysis of miscarriage products: an efficient and robust alternative to karyotype analysis.

Donaghue C, Mann K, Docherty Z, Mazzaschi R, Fear C, Ogilvie C. Donaghue C, et al. Among authors: docherty z. Prenat Diagn. 2010 Feb;30(2):133-7. doi: 10.1002/pd.2424. Prenat Diagn. 2010. PMID: 20024950

2

Strategies for the rapid prenatal diagnosis of chromosome aneuploidy.

Mann K, Donaghue C, Fox SP, Docherty Z, Ogilvie CM. Mann K, et al. Among authors: docherty z. Eur J Hum Genet. 2004 Nov;12(11):907-15. doi: 10.1038/sj.ejhg.5201224. Eur J Hum Genet. 2004. PMID: 15292918

3

Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping.

Stojilkovic-Mikic T, Mann K, Docherty Z, Mackie Ogilvie C. Stojilkovic-Mikic T, et al. Among authors: docherty z. Prenat Diagn. 2005 Jan;25(1):79-83. doi: 10.1002/pd.1089. Prenat Diagn. 2005. PMID: 15662689

4

Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.

Donaghue C, Mann K, Docherty Z, Ogilvie CM. Donaghue C, et al. Among authors: docherty z. Prenat Diagn. 2005 Jan;25(1):65-72. doi: 10.1002/pd.1086. Prenat Diagn. 2005. PMID: 15662691

5

Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).

Ogilvie CM, Donaghue C, Fox SP, Docherty Z, Mann K. Ogilvie CM, et al. Among authors: docherty z. J Histochem Cytochem. 2005 Mar;53(3):285-8. doi: 10.1369/jhc.4B6409.2005. J Histochem Cytochem. 2005. PMID: 15750003

6

QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region.

Hills A, Donaghue C, Waters J, Waters K, Sullivan C, Kulkarni A, Docherty Z, Mann K, Ogilvie CM. Hills A, et al. Among authors: docherty z. Prenat Diagn. 2010 Jun;30(6):509-17. doi: 10.1002/pd.2503. Prenat Diagn. 2010. PMID: 20509149

7

Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis.

Mann K, Fox SP, Abbs SJ, Yau SC, Scriven PN, Docherty Z, Ogilvie CM. Mann K, et al. Among authors: docherty z. Lancet. 2001 Sep 29;358(9287):1057-61. doi: 10.1016/S0140-6736(01)06183-9. Lancet. 2001. PMID: 11589937

8

Submicroscopic chromosome imbalance in patients with developmental delay and/or dysmorphism referred specifically for Fragile X testing and karyotype analysis.

Ahn JW, Mann K, Docherty Z, Mackie Ogilvie C. Ahn JW, et al. Among authors: docherty z. Mol Cytogenet. 2008 Mar 26;1:2. doi: 10.1186/1755-8166-1-2. Mol Cytogenet. 2008. PMID: 18471307 Free PMC article.

9

Characterization of terminal chromosome anomalies using multisubtelomere FISH.

Davies AF, Kirby TL, Docherty Z, Ogilvie CM. Davies AF, et al. Among authors: docherty z. Am J Med Genet A. 2003 Aug 1;120A(4):483-9. doi: 10.1002/ajmg.a.20056. Am J Med Genet A. 2003. PMID: 12884426

10

An Evaluation of the Effectiveness of a Semi-automatic Metaphase Locating and On-screen Karyotyping System.

May PC, Ogilvie CM, Mohammed S, Docherty Z, Hall RP. May PC, et al. Among authors: docherty z. J Assoc Genet Technol. 2008;34(4):177-87. J Assoc Genet Technol. 2008. PMID: 20081315

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