Crolla JA - Search Results

1

Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosis.

White HE, Dent CL, Hall VJ, Crolla JA, Chitty LS. White HE, et al. Among authors: crolla ja. PLoS One. 2012;7(9):e45073. doi: 10.1371/journal.pone.0045073. Epub 2012 Sep 14. PLoS One. 2012. PMID: 23024794 Free PMC article.

2

The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature.

Callaway JL, Shaffer LG, Chitty LS, Rosenfeld JA, Crolla JA. Callaway JL, et al. Among authors: crolla ja. Prenat Diagn. 2013 Dec;33(12):1119-23. doi: 10.1002/pd.4209. Epub 2013 Sep 8. Prenat Diagn. 2013. PMID: 23983223 Free PMC article. Review.

3

Evaluation of Array Comparative genomic Hybridisation in prenatal diagnosis of fetal anomalies: a multicentre cohort study with cost analysis and assessment of patient, health professional and commissioner preferences for array comparative genomic hybridisation.

Robson SC, Chitty LS, Morris S, Verhoef T, Ambler G, Wellesley DG, Graham R, Leader C, Fisher J, Crolla JA. Robson SC, et al. Among authors: crolla ja. Southampton (UK): NIHR Journals Library; 2017 Feb. Southampton (UK): NIHR Journals Library; 2017 Feb. PMID: 28182369 Free Books & Documents. Review.

4

Controversies in prenatal diagnosis 3: should everyone undergoing invasive testing have a microarray?

Crolla JA, Wapner R, Van Lith JM. Crolla JA, et al. Prenat Diagn. 2014 Jan;34(1):18-22. doi: 10.1002/pd.4287. Prenat Diagn. 2014. PMID: 24302430 No abstract available.

5

Perspective on the technical challenges involved in the implementation of array-CGH in prenatal diagnostic testing.

Callaway JL, Huang S, Karampetsou E, Crolla JA. Callaway JL, et al. Among authors: crolla ja. Mol Biotechnol. 2014 Apr;56(4):312-8. doi: 10.1007/s12033-013-9710-4. Mol Biotechnol. 2014. PMID: 24146428

6

FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases.

Crolla JA, Long F, Rivera H, Dennis NR. Crolla JA, et al. Am J Med Genet. 1998 Feb 3;75(4):355-66. doi: 10.1002/(sici)1096-8628(19980203)75:4<355::aid-ajmg4>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9482641

7

A molecular and FISH analysis of structurally abnormal Y chromosomes in patients with Turner syndrome.

Robinson DO, Dalton P, Jacobs PA, Mosse K, Power MM, Skuse DH, Crolla JA. Robinson DO, et al. Among authors: crolla ja. J Med Genet. 1999 Apr;36(4):279-84. J Med Genet. 1999. PMID: 10227393 Free PMC article.

8

Triplication of 15q11-q13 with inv dup(15) in a female with developmental delay.

Long FL, Duckett DP, Billam LJ, Williams DK, Crolla JA. Long FL, et al. Among authors: crolla ja. J Med Genet. 1998 May;35(5):425-8. doi: 10.1136/jmg.35.5.425. J Med Genet. 1998. PMID: 9610809 Free PMC article.

9

Molecular and fluorescence in situ hybridization characterization of the breakpoints in 46 large supernumerary marker 15 chromosomes reveals an unexpected level of complexity.

Roberts SE, Maggouta F, Thomas NS, Jacobs PA, Crolla JA. Roberts SE, et al. Among authors: crolla ja. Am J Hum Genet. 2003 Nov;73(5):1061-72. doi: 10.1086/379155. Epub 2003 Oct 14. Am J Hum Genet. 2003. PMID: 14560400 Free PMC article.

10

A case of maternal uniparental disomy of chromosome 9 in association with confined placental mosaicism for trisomy 9.

Wilkinson TA, James RS, Crolla JA, Cockwell AE, Campbell PL, Temple IK. Wilkinson TA, et al. Among authors: crolla ja. Prenat Diagn. 1996 Apr;16(4):371-4. doi: 10.1002/(SICI)1097-0223(199604)16:4<371::AID-PD866>3.0.CO;2-S. Prenat Diagn. 1996. PMID: 8734817

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