Docherty Z - Search Results

1

Novel deletion variants of 9q13-q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin.

Willatt LR, Barber JC, Clarkson A, Simonic I, Raymond FL, Docherty Z, Ogilvie CM. Willatt LR, et al. Among authors: docherty z. Eur J Hum Genet. 2007 Jan;15(1):45-52. doi: 10.1038/sj.ejhg.5201720. Epub 2006 Sep 20. Eur J Hum Genet. 2007. PMID: 16985501

2

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

3

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

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

A new approach to the elucidation of complex chromosome rearrangements illustrated by a case of Rieger syndrome.

Ogilvie CM, Raymond FL, Harrison RH, Scriven PN, Docherty Z. Ogilvie CM, et al. Among authors: docherty z. J Med Genet. 1998 Mar;35(3):234-7. doi: 10.1136/jmg.35.3.234. J Med Genet. 1998. PMID: 9541109 Free PMC article.

6

Chromosome 22q11 deletions are not found in autistic patients identified using strict diagnostic criteria. IMGSAC. International Molecular Genetics Study of Autism Consortium.

Ogilvie CM, Moore J, Daker M, Palferman S, Docherty Z. Ogilvie CM, et al. Among authors: docherty z. Am J Med Genet. 2000 Feb 7;96(1):15-7. Am J Med Genet. 2000. PMID: 10686546

7

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

8

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

9

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

10

Clinical expression of Menkes disease in a girl with X;13 translocation.

Abusaad I, Mohammed SN, Ogilvie CM, Ritchie J, Pohl KR, Docherty Z. Abusaad I, et al. Among authors: docherty z. Am J Med Genet. 1999 Dec 3;87(4):354-9. Am J Med Genet. 1999. PMID: 10588844

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