Hefferton D - Search Results

1

A founder effect in the newfoundland population reduces the Bardet-Biedl syndrome I (BBS1) interval to 1 cM.

Young TL, Woods MO, Parfrey PS, Green JS, Hefferton D, Davidson WS. Young TL, et al. Among authors: hefferton d. Am J Hum Genet. 1999 Dec;65(6):1680-7. doi: 10.1086/302686. Am J Hum Genet. 1999. PMID: 10577922 Free PMC article.

2

The importance of renal impairment in the natural history of Bardet-Biedl syndrome.

O'Dea D, Parfrey PS, Harnett JD, Hefferton D, Cramer BC, Green J. O'Dea D, et al. Among authors: hefferton d. Am J Kidney Dis. 1996 Jun;27(6):776-83. doi: 10.1016/s0272-6386(96)90513-2. Am J Kidney Dis. 1996. PMID: 8651240

3

Canadian Bardet-Biedl syndrome family reduces the critical region of BBS3 (3p) and presents with a variable phenotype.

Young TL, Woods MO, Parfrey PS, Green JS, O'Leary E, Hefferton D, Davidson WS. Young TL, et al. Among authors: hefferton d. Am J Med Genet. 1998 Aug 6;78(5):461-7. doi: 10.1002/(sici)1096-8628(19980806)78:5<461::aid-ajmg12>3.0.co;2-d. Am J Med Genet. 1998. PMID: 9714014

4

Genetic heterogeneity of Bardet-Biedl syndrome in a distinct Canadian population: evidence for a fifth locus.

Woods MO, Young TL, Parfrey PS, Hefferton D, Green JS, Davidson WS. Woods MO, et al. Among authors: hefferton d. Genomics. 1999 Jan 1;55(1):2-9. doi: 10.1006/geno.1998.5626. Genomics. 1999. PMID: 9888993

5

A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31.

Young TL, Penney L, Woods MO, Parfrey PS, Green JS, Hefferton D, Davidson WS. Young TL, et al. Among authors: hefferton d. Am J Hum Genet. 1999 Mar;64(3):900-4. doi: 10.1086/302301. Am J Hum Genet. 1999. PMID: 10053027 Free PMC article. No abstract available.

6

Bardet-Biedl syndrome 1 genotype and obesity in the Newfoundland population.

Fan Y, Rahman P, Peddle L, Hefferton D, Gladney N, Moore SJ, Green JS, Parfrey PS, Davidson WS. Fan Y, et al. Among authors: hefferton d. Int J Obes Relat Metab Disord. 2004 May;28(5):680-4. doi: 10.1038/sj.ijo.0802601. Int J Obes Relat Metab Disord. 2004. PMID: 14993910

7

Familial risk of preeclampsia in Newfoundland: a population-based study.

Dawson LM, Parfrey PS, Hefferton D, Dicks EL, Cooper MJ, Young D, Marsden PA. Dawson LM, et al. Among authors: hefferton d. J Am Soc Nephrol. 2002 Jul;13(7):1901-6. doi: 10.1097/01.asn.0000017224.24670.82. J Am Soc Nephrol. 2002. PMID: 12089387

8

Higher risk for renal failure in first-degree relatives of white patients with end-stage renal disease: a population-based study.

O'Dea DF, Murphy SW, Hefferton D, Parfrey PS. O'Dea DF, et al. Among authors: hefferton d. Am J Kidney Dis. 1998 Nov;32(5):794-801. doi: 10.1016/s0272-6386(98)70135-0. Am J Kidney Dis. 1998. PMID: 9820449

9

Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney disease.

Pei Y, Paterson AD, Wang KR, He N, Hefferton D, Watnick T, Germino GG, Parfrey P, Somlo S, St George-Hyslop P. Pei Y, et al. Among authors: hefferton d. Am J Hum Genet. 2001 Feb;68(2):355-63. doi: 10.1086/318188. Epub 2001 Jan 10. Am J Hum Genet. 2001. PMID: 11156533 Free PMC article.

10

Advance prediction of early death in patients starting maintenance dialysis.

Foley RN, Parfrey PS, Hefferton D, Singh I, Simms A, Barrett BJ. Foley RN, et al. Among authors: hefferton d. Am J Kidney Dis. 1994 Jun;23(6):836-45. doi: 10.1016/s0272-6386(12)80137-5. Am J Kidney Dis. 1994. PMID: 8203366

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