Crolla JA - Search Results

1

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.

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 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.

4

Further case of trisomy 18 mosaicism with a mild phenotype.

Collins AL, Fisher J, Crolla JA, Cockwell AE. Collins AL, et al. Among authors: crolla ja. Am J Med Genet. 1995 Mar 13;56(1):121-2. doi: 10.1002/ajmg.1320560129. Am J Med Genet. 1995. PMID: 7747777 No abstract available.

5

Genetic abnormalities detected in ependymomas by comparative genomic hybridisation.

Carter M, Nicholson J, Ross F, Crolla J, Allibone R, Balaji V, Perry R, Walker D, Gilbertson R, Ellison DW. Carter M, et al. Br J Cancer. 2002 Mar 18;86(6):929-39. doi: 10.1038/sj.bjc.6600180. Br J Cancer. 2002. PMID: 11953826 Free PMC article.

6

Breakpoint mapping and array CGH in translocations: comparison of a phenotypically normal and an abnormal cohort.

Baptista J, Mercer C, Prigmore E, Gribble SM, Carter NP, Maloney V, Thomas NS, Jacobs PA, Crolla JA. Baptista J, et al. Among authors: crolla ja. Am J Hum Genet. 2008 Apr;82(4):927-36. doi: 10.1016/j.ajhg.2008.02.012. Epub 2008 Mar 27. Am J Hum Genet. 2008. PMID: 18371933 Free PMC article.

7

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.

8

Rapid in situ harvesting and cytogenetic analysis of perinatal tissue samples.

Fisher AM, Cockwell AE, Moore KJ, Gregson NM, Campbell PL, Campbell CM, Herbert A, Barber JC, Crolla JA. Fisher AM, et al. Among authors: crolla ja. Prenat Diagn. 1996 Jul;16(7):615-21. doi: 10.1002/(SICI)1097-0223(199607)16:7<615::AID-PD920>3.0.CO;2-9. Prenat Diagn. 1996. PMID: 8843470

9

De novo deletions and duplications detected by array CGH: a study of parental origin in relation to mechanisms of formation and size of imbalance.

Sibbons C, Morris JK, Crolla JA, Jacobs PA, Thomas NS. Sibbons C, et al. Among authors: crolla ja. Eur J Hum Genet. 2012 Feb;20(2):155-60. doi: 10.1038/ejhg.2011.182. Epub 2011 Sep 28. Eur J Hum Genet. 2012. PMID: 21952720 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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