Wilson D - Search Results

1

Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11.

Carey AH, Claussen U, Lüdecke HJ, Horsthemke B, Ellis D, Oakey H, Wilson D, Burn J, Williamson R, Scambler PJ. Carey AH, et al. Among authors: wilson d. Mamm Genome. 1992;3(2):101-5. doi: 10.1007/BF00431253. Mamm Genome. 1992. PMID: 1617213

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: wilson di. 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. Lancet. 1992 Sep 5;340(8819):573-5. doi: 10.1016/0140-6736(92)92107-q. Lancet. 1992. PMID: 1355155

4

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. Am J Hum Genet. 1992 Nov;51(5):957-63. Am J Hum Genet. 1992. PMID: 1415264 Free PMC article.

5

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: wilson d. Am J Hum Genet. 1992 Nov;51(5):964-70. Am J Hum Genet. 1992. PMID: 1415265 Free PMC article.

6

Isolation of anonymous DNA markers for human chromosome 22q11 from a flow-sorted library, and mapping using hybrids from patients with DiGeorge syndrome.

Sharkey AM, McLaren L, Carroll M, Fantes J, Green D, Wilson D, Scambler PJ, Evans HJ. Sharkey AM, et al. Among authors: wilson d. Hum Genet. 1992 Apr;89(1):73-8. doi: 10.1007/BF00207046. Hum Genet. 1992. PMID: 1577468

7

DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.

Wilson DI, Cross IE, Goodship JA, Coulthard S, Carey AH, Scambler PJ, Bain HH, Hunter AS, Carter PE, Burn J. Wilson DI, et al. Br Heart J. 1991 Oct;66(4):308-12. doi: 10.1136/hrt.66.4.308. Br Heart J. 1991. PMID: 1747284 Free PMC article.

8

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: wilson d. Hum Mol Genet. 1995 Jun;4(6):1027-33. doi: 10.1093/hmg/4.6.1027. Hum Mol Genet. 1995. PMID: 7655455

9

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: wilson d. 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.

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: wilson d. 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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