Casey G - Search Results

1

Genetic susceptibility to viral exposure may increase the risk of cerebral palsy.

Djukic M, Gibson CS, Maclennan AH, Goldwater PN, Haan EA, McMichael G, Priest K, Dekker GA, Hague WM, Chan A, Rudzki Z, VAN Essen P, Khong TY, Morton MR, Ranieri E, Scott H, Tapp H, Casey G. Djukic M, et al. Among authors: casey g. Aust N Z J Obstet Gynaecol. 2009 Jun;49(3):247-53. doi: 10.1111/j.1479-828X.2009.00999.x. Aust N Z J Obstet Gynaecol. 2009. PMID: 19566553

2

Detection of rearrangement within the breakpoint cluster region of chromosome 22 in the diagnosis of chronic myeloid leukemia.

Hutchins C, Casey G, White D, Moore S, Rudzki Z, Kimber R. Hutchins C, et al. Among authors: casey g. Aust N Z J Med. 1989 Oct;19(5):443-8. doi: 10.1111/j.1445-5994.1989.tb00302.x. Aust N Z J Med. 1989. PMID: 2590093

3

Demonstration of a recent mutation in a family with isolated hemophilia A.

Rudzki Z, Rodgers SE, Casey G, Mulley JC, Sutherland GR, Lloyd JV. Rudzki Z, et al. Among authors: casey g. Aust N Z J Med. 1987 Dec;17(6):609-10. doi: 10.1111/j.1445-5994.1987.tb01272.x. Aust N Z J Med. 1987. PMID: 2895997 No abstract available.

4

Grandpaternal mosaicism in a family with isolated haemophilia A.

Casey GJ, Rodgers SE, Hall JR, Rudzki Z, Lloyd JV. Casey GJ, et al. Br J Haematol. 1999 Dec;107(3):560-2. doi: 10.1046/j.1365-2141.1999.01743.x. Br J Haematol. 1999. PMID: 10583258 Free article.

5

Direct mutation analysis as the preferred method for carrier diagnosis in families with isolated cases of haemophilia B.

Andrews AE, Casey GJ, Rodgers SE, Flower RL, Rudzki Z. Andrews AE, et al. Among authors: casey gj. Haemophilia. 1996 Oct;2(4):196-201. doi: 10.1111/j.1365-2516.1996.tb00136.x. Haemophilia. 1996. PMID: 27214356

6

N-ras mutation in acute myeloid leukemia: incidence, prognostic significance and value as a marker of minimal residual disease.

Casey G, Rudzki Z, Roberts M, Hutchins C, Juttner C. Casey G, et al. Pathology. 1993 Jan;25(1):57-62. doi: 10.3109/00313029309068903. Pathology. 1993. PMID: 8316501

7

Mutations in a subgroup of patients with mild haemophilia A and a familial discrepancy between the one-stage and two-stage factor VIII:C methods.

Rudzki Z, Duncan EM, Casey GJ, Neumann M, Favaloro EJ, Lloyd JV. Rudzki Z, et al. Among authors: casey gj. Br J Haematol. 1996 Aug;94(2):400-6. doi: 10.1046/j.1365-2141.1996.d01-1792.x. Br J Haematol. 1996. PMID: 8759905

8

Microsatellite instability markers in breast cancer: a review and study showing MSI was not detected at 'BAT 25' and 'BAT 26' microsatellite markers in early-onset breast cancer.

Siah SP, Quinn DM, Bennett GD, Casey G, Flower RL, Suthers G, Rudzki Z. Siah SP, et al. Among authors: casey g. Breast Cancer Res Treat. 2000 Mar;60(2):135-42. doi: 10.1023/a:1006315315060. Breast Cancer Res Treat. 2000. PMID: 10845276 Review.

9

Detection of paternally inherited mutations for beta-thalassemia in trophoblast isolated from peripheral maternal blood.

Hawes CS, Suskin HA, Kalionis B, Mueller UW, Casey G, Hall J, Rudzki Z. Hawes CS, et al. Among authors: casey g. Ann N Y Acad Sci. 1994 Sep 7;731:181-5. doi: 10.1111/j.1749-6632.1994.tb55767.x. Ann N Y Acad Sci. 1994. PMID: 7944116 No abstract available.

10

Familial vasopressin-sensitive ACTH-independent macronodular adrenal hyperplasia (VPs-AIMAH): clinical studies of three kindreds.

Gagliardi L, Hotu C, Casey G, Braund WJ, Ling KH, Dodd T, Manavis J, Devitt PG, Cutfield R, Rudzki Z, Scott HS, Torpy DJ. Gagliardi L, et al. Among authors: casey g. Clin Endocrinol (Oxf). 2009 Jun;70(6):883-91. doi: 10.1111/j.1365-2265.2008.03471.x. Epub 2008 Nov 5. Clin Endocrinol (Oxf). 2009. PMID: 19018784

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