Goodship J - Search Results

1

Early confirmation of trisomy 18 in newborn babies.

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

2

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus.

Scambler PJ, Kelly D, Lindsay E, Williamson R, Goldberg R, Shprintzen R, Wilson DI, Goodship JA, Cross IE, Burn J. Scambler PJ, et al. Among authors: goodship ja. Lancet. 1992 May 9;339(8802):1138-9. doi: 10.1016/0140-6736(92)90734-k. Lancet. 1992. PMID: 1349369

3

Deletions within chromosome 22q11 in familial congenital heart disease.

Wilson DI, Goodship JA, Burn J, Cross IE, Scambler PJ. Wilson DI, et al. Among authors: goodship ja. Lancet. 1992 Sep 5;340(8819):573-5. doi: 10.1016/0140-6736(92)92107-q. Lancet. 1992. PMID: 1355155

4

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: goodship ja. 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.

5

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: goodship j. Prenat Diagn. 1998 Jul;18(7):737-41. Prenat Diagn. 1998. PMID: 9706657

6

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: goodship ja. 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

7

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

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

8

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. Among authors: goodship ja. Prenat Diagn. 2001 Oct;21(10):813-7. doi: 10.1002/pd.143. Prenat Diagn. 2001. PMID: 11746120

9

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: goodship j. Prenat Diagn. 1995 Aug;15(8):773-7. doi: 10.1002/pd.1970150816. Prenat Diagn. 1995. PMID: 7479599

10

Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11.

Kelly D, Goldberg R, Wilson D, Lindsay E, Carey A, Goodship J, Burn J, Cross I, Shprintzen RJ, Scambler PJ. Kelly D, et al. Among authors: goodship j. Am J Med Genet. 1993 Feb 1;45(3):308-12. doi: 10.1002/ajmg.1320450306. Am J Med Genet. 1993. PMID: 8434616

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