Goodship J - Search Results

1

Isolation of a gene encoding an integral membrane protein from the vicinity of a balanced translocation breakpoint associated with DiGeorge syndrome.

Wadey R, Daw S, Taylor C, Atif U, Kamath S, Halford S, O'Donnell H, Wilson D, Goodship J, Burn J, et al. Wadey R, et al. Among authors: goodship j. Hum Mol Genet. 1995 Jun;4(6):1027-33. doi: 10.1093/hmg/4.6.1027. Hum Mol Genet. 1995. PMID: 7655455

2

Molecular genetic study of the frequency of monosomy 22q11 in DiGeorge syndrome.

Carey AH, Kelly D, Halford S, Wadey R, Wilson D, Goodship J, Burn J, Paul T, Sharkey A, Dumanski J, et al. Carey AH, et al. Among authors: goodship j. Am J Hum Genet. 1992 Nov;51(5):964-70. Am J Hum Genet. 1992. PMID: 1415265 Free PMC article.

3

Isolation of a new marker and conserved sequences close to the DiGeorge syndrome marker HP500 (D22S134).

Wadey R, Daw S, Wickremasinghe A, Roberts C, Wilson D, Goodship J, Burn J, Halford S, Scambler PJ. Wadey R, et al. Among authors: goodship j. J Med Genet. 1993 Oct;30(10):818-21. doi: 10.1136/jmg.30.10.818. J Med Genet. 1993. PMID: 8230156 Free PMC article.

4

DiGeorge syndrome: part of CATCH 22.

Wilson DI, Burn J, Scambler P, Goodship J. Wilson DI, et al. Among authors: goodship j. J Med Genet. 1993 Oct;30(10):852-6. doi: 10.1136/jmg.30.10.852. J Med Genet. 1993. PMID: 8230162 Free PMC article.

5

Isolation of a gene expressed during early embryogenesis from the region of 22q11 commonly deleted in DiGeorge syndrome.

Halford S, Wilson DI, Daw SC, Roberts C, Wadey R, Kamath S, Wickremasinghe A, Burn J, Goodship J, Mattei MG, et al. Halford S, et al. Among authors: goodship j. Hum Mol Genet. 1993 Oct;2(10):1577-82. doi: 10.1093/hmg/2.10.1577. Hum Mol Genet. 1993. PMID: 8268909

6

Identification of a novel transcript disrupted by a balanced translocation associated with DiGeorge syndrome.

Sutherland HF, Wadey R, McKie JM, Taylor C, Atif U, Johnstone KA, Halford S, Kim UJ, Goodship J, Baldini A, Scambler PJ. Sutherland HF, et al. Among authors: goodship j. Am J Hum Genet. 1996 Jul;59(1):23-31. Am J Hum Genet. 1996. PMID: 8659529 Free PMC article.

7

A common region of 10p deleted in DiGeorge and velocardiofacial syndromes.

Daw SC, Taylor C, Kraman M, Call K, Mao J, Schuffenhauer S, Meitinger T, Lipson T, Goodship J, Scambler P. Daw SC, et al. Among authors: goodship j. Nat Genet. 1996 Aug;13(4):458-60. doi: 10.1038/ng0896-458. Nat Genet. 1996. PMID: 8696341

8

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

9

A prospective cytogenetic study of 36 cases of DiGeorge syndrome.

Wilson DI, Cross IE, Goodship JA, Brown J, Scambler PJ, Bain HH, Taylor JF, Walsh K, Bankier A, Burn J, et al. Wilson DI, et al. Among authors: goodship ja. Am J Hum Genet. 1992 Nov;51(5):957-63. Am J Hum Genet. 1992. PMID: 1415264 Free PMC article.

10

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

Burn J, Takao A, Wilson D, Cross I, Momma K, Wadey R, Scambler P, Goodship J. Burn J, et al. Among authors: goodship j. J Med Genet. 1993 Oct;30(10):822-4. doi: 10.1136/jmg.30.10.822. J Med Genet. 1993. PMID: 8230157 Free PMC article.

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