Graham CA - 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: graham ca. 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

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: graham ca. 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.

4

Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern Ireland.

Hill AJ, Graham CA, Kelly ED, Morrison PJ, Nevin NC. Hill AJ, et al. Among authors: graham ca. Hum Genet. 1989 Nov;83(4):391-4. doi: 10.1007/BF00291387. Hum Genet. 1989. PMID: 2572538

5

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: graham ca. Acta Paediatr Suppl. 1994 Dec;407:37-8. doi: 10.1111/j.1651-2227.1994.tb13445.x. Acta Paediatr Suppl. 1994. PMID: 7766952

6

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: graham ca. Acta Paediatr Suppl. 1994 Dec;407:41-2. doi: 10.1111/j.1651-2227.1994.tb13447.x. Acta Paediatr Suppl. 1994. PMID: 7766955

7

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: graham ca. 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.

8

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: graham ca. Hum Mutat. 1994;4(2):114-8. doi: 10.1002/humu.1380040204. Hum Mutat. 1994. PMID: 7981714

9

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: graham ca. 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.

10

Three novel mutations in the EGF precursor homology domain of the low-density lipoprotein receptor gene in Northern Irish patients with familial hypercholesterolemia.

Ward AJ, O'Kane M, Young I, Nicholls DP, Nevin NC, Graham CA. Ward AJ, et al. Among authors: graham ca. Hum Mutat. 1995;6(3):254-6. doi: 10.1002/humu.1380060311. Hum Mutat. 1995. PMID: 8535447 No abstract available.

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