Wolstenholme J - Search Results

1

Early confirmation of trisomy 18 in newborn babies.

Wolstenholme J, Cross I, Goodship J. Wolstenholme J, et al. Lancet. 1992 Jun 6;339(8806):1416. doi: 10.1016/0140-6736(92)91236-2. Lancet. 1992. PMID: 1350825 No abstract available.

2

Trisomy 12 mosaicism in a 7 year old girl with dysmorphic features and normal mental development.

English CJ, Goodship JA, Jackson A, Lowry M, Wolstenholme J. English CJ, et al. Among authors: wolstenholme j. J Med Genet. 1994 Mar;31(3):253-4. doi: 10.1136/jmg.31.3.253. J Med Genet. 1994. PMID: 8014979 Free PMC article. Review.

3

Prenatal diagnosis of mosaic trisomy 8 with investigations of the extent and origin of trisomic cells.

Webb AL, Wolstenholme J, Evans J, Macphail S, Goodship J. Webb AL, et al. Among authors: wolstenholme j. Prenat Diagn. 1998 Jul;18(7):737-41. Prenat Diagn. 1998. PMID: 9706657

4

Maternal uniparental disomy for chromosome 2 in association with confined placental mosaicism for trisomy 2 and severe intrauterine growth retardation.

Webb AL, Sturgiss S, Warwicker P, Robson SC, Goodship JA, Wolstenholme J. Webb AL, et al. Among authors: wolstenholme j. Prenat Diagn. 1996 Oct;16(10):958-62. doi: 10.1002/(SICI)1097-0223(199610)16:10<958::AID-PD971>3.0.CO;2-U. Prenat Diagn. 1996. PMID: 8938070

5

Prenatal detection of multiple copies of a familial supernumerary marker chromosome.

Wolstenholme J, Brummitt JA, English CJ, Goodship JA. Wolstenholme J, et al. Prenat Diagn. 1992 Dec;12(12):1067-71. doi: 10.1002/pd.1970121214. Prenat Diagn. 1992. PMID: 1287643 Review.

6

A case of paternal uniparental disomy for chromosome 11.

Webb A, Beard J, Wright C, Robson S, Wolstenholme J, Goodship J. Webb A, et al. Among authors: wolstenholme j. Prenat Diagn. 1995 Aug;15(8):773-7. doi: 10.1002/pd.1970150816. Prenat Diagn. 1995. PMID: 7479599

7

Maternal uniparental heterodisomy for chromosome 2: detection through 'atypical' maternal AFP/hCG levels, with an update on a previous case.

Wolstenholme J, White I, Sturgiss S, Carter J, Plant N, Goodship JA. Wolstenholme J, et al. Prenat Diagn. 2001 Oct;21(10):813-7. doi: 10.1002/pd.143. Prenat Diagn. 2001. PMID: 11746120

8

A submicroscopic translocation, t(4;10), responsible for recurrent Wolf-Hirschhorn syndrome identified by allele loss and fluorescent in situ hybridisation.

Goodship J, Curtis A, Cross I, Brown J, Emslie J, Wolstenholme J, Bhattacharya S, Burn J. Goodship J, et al. Among authors: wolstenholme j. J Med Genet. 1992 Jul;29(7):451-4. J Med Genet. 1992. PMID: 1640422 Free PMC article.

9

An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

Cross I, Delhanty J, Chapman P, Bowles LV, Griffin D, Wolstenholme J, Bradburn M, Brown J, Wood C, Gunn A, et al. Cross I, et al. Among authors: wolstenholme j. J Med Genet. 1992 Mar;29(3):175-9. doi: 10.1136/jmg.29.3.175. J Med Genet. 1992. PMID: 1313112 Free PMC article.

10

An audit of trisomy 16 in man.

Wolstenholme J. Wolstenholme J. Prenat Diagn. 1995 Feb;15(2):109-21. doi: 10.1002/pd.1970150202. Prenat Diagn. 1995. PMID: 7784361 Review.

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