MacLeod H - Search Results

1

Watson syndrome: is it a subtype of type 1 neurofibromatosis?

Allanson JE, Upadhyaya M, Watson GH, Partington M, MacKenzie A, Lahey D, MacLeod H, Sarfarazi M, Broadhead W, Harper PS, et al. Allanson JE, et al. Among authors: macleod h. J Med Genet. 1991 Nov;28(11):752-6. doi: 10.1136/jmg.28.11.752. J Med Genet. 1991. PMID: 1770531 Free PMC article.

2

DNA polymorphism and linkage disequilibrium within the apolipoprotein CII locus on human chromosome 19.

MacKenzie AE, MacLeod HL, Leblond SC, Monteith N, Lahey D, Korneluk RG. MacKenzie AE, et al. Among authors: macleod hl. Hum Hered. 1991;41(3):188-94. doi: 10.1159/000153999. Hum Hered. 1991. PMID: 1682238

3

Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.

MacKenzie AE, MacLeod HL, Hunter AG, Korneluk RG. MacKenzie AE, et al. Among authors: macleod hl. Am J Hum Genet. 1989 Jan;44(1):140-7. Am J Hum Genet. 1989. PMID: 2562820 Free PMC article.

4

A BanI polymorphism identified by the probe p alpha 1.4P at 19q13.1 [D19S37].

Korneluk RG, MacLeod HL, Lahey D, McKeithan TW, MacKenzie AE. Korneluk RG, et al. Among authors: macleod hl. Nucleic Acids Res. 1989 Jul 25;17(14):5874. doi: 10.1093/nar/17.14.5874. Nucleic Acids Res. 1989. PMID: 2569726 Free PMC article. No abstract available.

5

A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy.

Korneluk RG, MacLeod HL, McKeithan TW, Brooks JD, MacKenzie AE. Korneluk RG, et al. Among authors: macleod hl. Genomics. 1989 Feb;4(2):146-51. doi: 10.1016/0888-7543(89)90293-0. Genomics. 1989. PMID: 2567698

6

A Bsu36I RFLP detected by the chromosome 19q probe p alpha.5B [D19S36].

Korneluk RG, MacLeod HL, Leblond S, McKeithan TW, MacKenzie AE. Korneluk RG, et al. Among authors: macleod hl. Nucleic Acids Res. 1989 Jul 25;17(14):5875. doi: 10.1093/nar/17.14.5875. Nucleic Acids Res. 1989. PMID: 2569727 Free PMC article. No abstract available.

7

False positive results from the alanine loading test for ornithine carbamoyltransferase deficiency heterozygosity.

MacKenzie AE, MacLeod HL, Heick HM, Korneluk RG. MacKenzie AE, et al. Among authors: macleod hl. J Pediatr. 1989 Oct;115(4):605-8. doi: 10.1016/s0022-3476(89)80294-x. J Pediatr. 1989. PMID: 2795358 No abstract available.

8

Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.

Kean VM, Macleod HL, Thompson MW, Ray PN, Verellen-Dumoulin C, Worton RG. Kean VM, et al. Among authors: macleod hl. J Med Genet. 1986 Dec;23(6):491-3. doi: 10.1136/jmg.23.6.491. J Med Genet. 1986. PMID: 2879921 Free PMC article.

9

Assessment of a matched-pair instrument to examine doctor-patient communication skills in practising doctors.

Campbell C, Lockyer J, Laidlaw T, Macleod H. Campbell C, et al. Among authors: macleod h. Med Educ. 2007 Feb;41(2):123-9. doi: 10.1111/j.1365-2929.2006.02657.x. Med Educ. 2007. PMID: 17269944

10

AvaII RFLP at the human apolipoprotein CII (APO CII) gene locus.

Korneluk RG, MacLeod HL, Leblond SC, Monteith NL, Baralle FE, Hunter AG. Korneluk RG, et al. Among authors: macleod hl. Nucleic Acids Res. 1987 Aug 25;15(16):6769. doi: 10.1093/nar/15.16.6769. Nucleic Acids Res. 1987. PMID: 2888095 Free PMC article.

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