Nevin NC - Search Results

1

Allelic and locus heterogeneity in inherited venous malformations.

Calvert JT, Riney TJ, Kontos CD, Cha EH, Prieto VG, Shea CR, Berg JN, Nevin NC, Simpson SA, Pasyk KA, Speer MC, Peters KG, Marchuk DA. Calvert JT, et al. Among authors: nevin nc. Hum Mol Genet. 1999 Jul;8(7):1279-89. doi: 10.1093/hmg/8.7.1279. Hum Mol Genet. 1999. PMID: 10369874

2

Additional glomangioma families link to chromosome 1p: no evidence for genetic heterogeneity.

Calvert JT, Burns S, Riney TJ, Sahoo T, Orlow SJ, Nevin NC, Haisley-Royster C, Prose N, Simpson SA, Speer MC, Marchuk DA. Calvert JT, et al. Among authors: nevin nc. Hum Hered. 2001;51(3):180-2. doi: 10.1159/000053340. Hum Hered. 2001. PMID: 11173970

3

Deafness, onycho-osteodystrophy, mental retardation (DOOR) syndrome.

Nevin NC, Thomas PS, Calvert J, Reid MM. Nevin NC, et al. Am J Med Genet. 1982 Nov;13(3):325-32. doi: 10.1002/ajmg.1320130316. Am J Med Genet. 1982. PMID: 7180877 No abstract available.

4

Genetic linkage of familial expansile osteolysis to chromosome 18q.

Hughes AE, Shearman AM, Weber JL, Barr RJ, Wallace RG, Osterberg PH, Nevin NC, Mollan RA. Hughes AE, et al. Among authors: nevin nc. Hum Mol Genet. 1994 Feb;3(2):359-61. doi: 10.1093/hmg/3.2.359. Hum Mol Genet. 1994. PMID: 7911698

5

Phenylketonuria mutation analysis in Northern Ireland: a rapid stepwise approach.

Zschocke J, Graham CA, Carson DJ, Nevin NC. Zschocke J, et al. Among authors: nevin nc. Am J Hum Genet. 1995 Dec;57(6):1311-7. Am J Hum Genet. 1995. PMID: 8533759 Free PMC article.

6

Identification of a single base pair deletion (40 del G) in exon 1 of the ferrochelatase gene in patients with erythropoietic protoporphyria.

Todd DJ, Hughes AE, Ennis KT, Ward AJ, Burrows D, Nevin NC. Todd DJ, et al. Among authors: nevin nc. Hum Mol Genet. 1993 Sep;2(9):1495-6. doi: 10.1093/hmg/2.9.1495. Hum Mol Genet. 1993. PMID: 8242081 No abstract available.

7

Female germline mosaicism in tuberous sclerosis confirmed by molecular genetic analysis.

Yates JR, van Bakel I, Sepp T, Payne SJ, Webb DW, Nevin NC, Green AJ. Yates JR, et al. Among authors: nevin nc. Hum Mol Genet. 1997 Dec;6(13):2265-9. doi: 10.1093/hmg/6.13.2265. Hum Mol Genet. 1997. PMID: 9361032

8

Fluorescent multiplex microsatellites used to identify haplotype associations with 15 CFTR mutations in 124 Northern Irish CF families.

Hughes D, Hill A, Redmond A, Nevin N, Graham C. Hughes D, et al. Hum Genet. 1995 Apr;95(4):462-4. doi: 10.1007/BF00208979. Hum Genet. 1995. PMID: 7535745

9

An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis.

Irvine AD, Dolan OM, Hadden DR, Stewart FJ, Bingham EA, Nevin NC. Irvine AD, et al. Among authors: nevin nc. J Med Genet. 1996 Nov;33(11):972-4. doi: 10.1136/jmg.33.11.972. J Med Genet. 1996. PMID: 8950682 Free PMC article.

10

Melorheostosis in a family with autosomal dominant osteopoikilosis.

Nevin NC, Thomas PS, Davis RI, Cowie GH. Nevin NC, et al. Am J Med Genet. 1999 Feb 19;82(5):409-14. doi: 10.1002/(sici)1096-8628(19990219)82:5<409::aid-ajmg10>3.0.co;2-2. Am J Med Genet. 1999. PMID: 10069713

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

239 results

Search Page

Filters