Hunter AG - Search Results

1

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: hunter ag. Am J Hum Genet. 1989 Jan;44(1):140-7. Am J Hum Genet. 1989. PMID: 2562820 Free PMC article.

2

Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.

Hunter AG, Jacob P, O'Hoy K, MacDonald I, Mettler G, Tsilfidis C, Korneluk RG. Hunter AG, et al. Am J Med Genet. 1993 Feb 1;45(3):401-7. doi: 10.1002/ajmg.1320450330. Am J Med Genet. 1993. PMID: 8434633

3

Simpson-Golabi-Behmel syndrome associated with renal dysplasia and embryonal tumor: localization of the gene to Xqcen-q21.

Hughes-Benzie RM, Hunter AG, Allanson JE, Mackenzie AE. Hughes-Benzie RM, et al. Among authors: hunter ag. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):428-35. doi: 10.1002/ajmg.1320430165. Am J Med Genet. 1992. PMID: 1605222

4

A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus.

Korneluk RG, MacKenzie AE, Nakamura Y, Dubé I, Jacob P, Hunter AG. Korneluk RG, et al. Among authors: hunter ag. Genomics. 1989 Oct;5(3):596-604. doi: 10.1016/0888-7543(89)90028-1. Genomics. 1989. PMID: 2613241

5

Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission.

O'Hoy KL, Tsilfidis C, Mahadevan MS, Neville CE, Barceló J, Hunter AG, Korneluk RG. O'Hoy KL, et al. Among authors: hunter ag. Science. 1993 Feb 5;259(5096):809-12. doi: 10.1126/science.8094260. Science. 1993. PMID: 8094260

6

Simpson-Golabi-Behmel syndrome: genotype/phenotype analysis of 18 affected males from 7 unrelated families.

Hughes-Benzie RM, Pilia G, Xuan JY, Hunter AG, Chen E, Golabi M, Hurst JA, Kobori J, Marymee K, Pagon RA, Punnett HH, Schelley S, Tolmie JL, Wohlferd MM, Grossman T, Schlessinger D, MacKenzie AE. Hughes-Benzie RM, et al. Among authors: hunter ag. Am J Med Genet. 1996 Dec 11;66(2):227-34. doi: 10.1002/(SICI)1096-8628(19961211)66:2<227::AID-AJMG20>3.0.CO;2-U. Am J Med Genet. 1996. PMID: 8958336

7

Clinical application of the molecular diagnosis of spinal muscular atrophy: deletions of neuronal apoptosis inhibitor protein and survival motor neuron genes.

Somerville MJ, Hunter AG, Aubry HL, Korneluk RG, MacKenzie AE, Surh LC. Somerville MJ, et al. Among authors: hunter ag. Am J Med Genet. 1997 Mar 17;69(2):159-65. Am J Med Genet. 1997. PMID: 9056553

8

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: hunter ag. 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.

9

Linkage relationships of X-linked choroideremia to DXYS1 and DXS3.

MacDonald IM, Sandre RM, Wong P, Hunter AG, Tenniswood MP. MacDonald IM, et al. Among authors: hunter ag. Hum Genet. 1987 Nov;77(3):233-5. doi: 10.1007/BF00284475. Hum Genet. 1987. PMID: 2890569

10

Delivery of molecular genetic services within a health care system: time analysis of the clinical workload. The Molecular Genetic Study Group.

Surh LC, Wright PG, Cappelli M, Kasaboski A, Hastings VA, Hunter AG. Surh LC, et al. Among authors: hunter ag. Am J Hum Genet. 1995 Mar;56(3):760-8. Am J Hum Genet. 1995. PMID: 7887432 Free PMC article.

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