Hunter AG - Search Results

1

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

2

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

3

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

4

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.

5

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

6

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

7

Mosaic r(13) in an infant with aprosencephaly.

Goldsmith CL, Tawagi GF, Carpenter BF, Speevak MD, Hunter AG. Goldsmith CL, et al. Among authors: hunter ag. Am J Med Genet. 1993 Sep 15;47(4):531-3. doi: 10.1002/ajmg.1320470418. Am J Med Genet. 1993. PMID: 8256818

8

Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis.

Wang H, McLaughlin M, Thompson C, Hunter AG. Wang H, et al. Among authors: hunter ag. Am J Med Genet. 1993 Jun 15;46(5):559-62. doi: 10.1002/ajmg.1320460520. Am J Med Genet. 1993. PMID: 8322821

9

VACTERL with hydrocephalus: spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance.

Wang H, Hunter AG, Clifford B, McLaughlin M, Thompson D. Wang H, et al. Among authors: hunter ag. Am J Med Genet. 1993 Aug 1;47(1):114-7. doi: 10.1002/ajmg.1320470124. Am J Med Genet. 1993. PMID: 8368240

10

Renal tubular dysgenesis: a not uncommon autosomal recessive syndrome: a review.

Allanson JE, Hunter AG, Mettler GS, Jimenez C. Allanson JE, et al. Among authors: hunter ag. Am J Med Genet. 1992 Jul 15;43(5):811-4. doi: 10.1002/ajmg.1320430512. Am J Med Genet. 1992. PMID: 1642268 Review.

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