Nevin NC - Search Results

1

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.

2

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

3

Detection of maternal cell contamination in amniotic fluid cell cultures using fluorescent labelled microsatellites.

Smith GW, Graham CA, Nevin J, Nevin NC. Smith GW, et al. Among authors: nevin j, nevin nc. J Med Genet. 1995 Jan;32(1):61-4. doi: 10.1136/jmg.32.1.61. J Med Genet. 1995. PMID: 7897630 Free PMC article.

4

Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosis.

Zschocke J, Graham CA, Stewart FJ, Carson DJ, Nevin NC. Zschocke J, et al. Among authors: nevin nc. Hum Mutat. 1994;4(2):114-8. doi: 10.1002/humu.1380040204. Hum Mutat. 1994. PMID: 7981714

5

Significant linkage disequilibrium between the Huntington's disease locus and markers at loci D4S10, D4S95, and D4S111 in Northern Ireland.

Morrison PJ, Graham CA, Nevin NC. Morrison PJ, et al. Among authors: nevin nc. J Med Genet. 1993 Dec;30(12):1018-9. doi: 10.1136/jmg.30.12.1018. J Med Genet. 1993. PMID: 8133499 Free PMC article.

6

Mutation characterization of CFTR gene in 206 Northern Irish CF families: thirty mutations, including two novel, account for approximately 94% of CF chromosomes.

Hughes DJ, Hill AJ, Macek M Jr, Redmond AO, Nevin NC, Graham CA. Hughes DJ, et al. Among authors: nevin nc. Hum Mutat. 1996;8(4):340-7. doi: 10.1002/(SICI)1098-1004(1996)8:4<340::AID-HUMU7>3.0.CO;2-B. Hum Mutat. 1996. PMID: 8956039

7

Phenylketonuria and the peoples of Northern Ireland.

Zschocke J, Mallory JP, Eiken HG, Nevin NC. Zschocke J, et al. Among authors: nevin nc. Hum Genet. 1997 Aug;100(2):189-94. doi: 10.1007/s004390050488. Hum Genet. 1997. PMID: 9254847

8

Automated sequencing detects all mutations in Northern Irish patients with phenylketonuria and mild hyperphenylalaninaemia.

Zschocke J, Graham CA, Stewart FJ, Carson DJ, Nevin NC. Zschocke J, et al. Among authors: nevin nc. Acta Paediatr Suppl. 1994 Dec;407:37-8. doi: 10.1111/j.1651-2227.1994.tb13445.x. Acta Paediatr Suppl. 1994. PMID: 7766952

9

The STR system in the human phenylalanine hydroxylase gene: true fragment length obtained with fluorescent labelled PCR primers.

Zschocke J, Graham CA, McKnight JJ, Nevin NC. Zschocke J, et al. Among authors: nevin nc. Acta Paediatr Suppl. 1994 Dec;407:41-2. doi: 10.1111/j.1651-2227.1994.tb13447.x. Acta Paediatr Suppl. 1994. PMID: 7766955

10

Carrier estimations in Duchenne muscular dystrophy families in Northern Ireland using RFLP analysis.

Kelly ED, Graham CA, Hill AJ, Nevin NC. Kelly ED, et al. Among authors: nevin nc. J Med Genet. 1990 Feb;27(2):101-4. doi: 10.1136/jmg.27.2.101. J Med Genet. 1990. PMID: 1969486 Free PMC article.

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