Hyland VJ - Search Results

1

Solid-phase amplification for detection of C282y and H63D hemochromatosis (HFE) gene mutations.

Turner MS, Penning S, Sharp A, Hyland VJ, Harris R, Morris CP, van Daal A. Turner MS, et al. Among authors: hyland vj. Clin Chem. 2001 Aug;47(8):1384-9. Clin Chem. 2001. PMID: 11468226

2

Genetic mapping of new RFLPs at Xq27-q28.

Suthers GK, Oberlé I, Nancarrow J, Mulley JC, Hyland VJ, Wilson PJ, McCure J, Morris CP, Hopwood JJ, Mandel JL, et al. Suthers GK, et al. Among authors: hyland vj. Genomics. 1991 Jan;9(1):37-43. doi: 10.1016/0888-7543(91)90218-4. Genomics. 1991. PMID: 1672291

3

Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.

Suthers GK, Hyland VJ, Callen DF, Oberle I, Rocchi M, Thomas NS, Morris CP, Schwartz CE, Schmidt M, Ropers HH, et al. Suthers GK, et al. Among authors: hyland vj. Am J Hum Genet. 1990 Aug;47(2):187-95. Am J Hum Genet. 1990. PMID: 2378346 Free PMC article.

4

Molecular detection of prostate cells in ejaculate and urethral washings in men with suspected prostate cancer.

Clements JA, Rohde P, Allen V, Hyland VJ, Samaratunga ML, Tilley WD, Lavin MF, Gardiner RA. Clements JA, et al. Among authors: hyland vj. J Urol. 1999 Apr;161(4):1337-43. J Urol. 1999. PMID: 10081904

5

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.

Chuah TL, Tan KM, Flanagan S, Hyland V, Sullivan AA, Henderson R, MacMillan J, Lander C. Chuah TL, et al. J Clin Neurosci. 2001 Sep;8(5):404-6. doi: 10.1054/jocn.2000.0848. J Clin Neurosci. 2001. PMID: 11535004

6

Mapping the short arm of human chromosome 16.

Callen DF, Hyland VJ, Baker EG, Fratini A, Gedeon AK, Mulley JC, Fernandez KE, Breuning MH, Sutherland GR. Callen DF, et al. Among authors: hyland vj. Genomics. 1989 Apr;4(3):348-54. doi: 10.1016/0888-7543(89)90341-8. Genomics. 1989. PMID: 2714795

7

Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16.

Callen DF, Hyland VJ, Baker EG, Fratini A, Simmers RN, Mulley JC, Sutherland GR. Callen DF, et al. Among authors: hyland vj. Genomics. 1988 Feb;2(2):144-53. doi: 10.1016/0888-7543(88)90096-1. Genomics. 1988. PMID: 2900808

8

Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1.

Hyland VJ, Suthers GK, Friend K, MacKinnon RN, Callen DF, Breuning MH, Keith T, Brown VA, Phipps P, Sutherland GR. Hyland VJ, et al. Hum Genet. 1990 Feb;84(3):286-8. doi: 10.1007/BF00200577. Hum Genet. 1990. PMID: 1968038

9

Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.

Richards RI, Shen Y, Holman K, Kozman H, Hyland VJ, Mulley JC, Sutherland GR. Richards RI, et al. Among authors: hyland vj. Am J Hum Genet. 1991 Jun;48(6):1051-7. Am J Hum Genet. 1991. PMID: 2035525 Free PMC article.

10

Molecular genetics of human chromosome 16.

Sutherland GR, Reeders S, Hyland VJ, Callen DF, Fratini A, Mulley JC. Sutherland GR, et al. Among authors: hyland vj. J Med Genet. 1987 Aug;24(8):451-6. doi: 10.1136/jmg.24.8.451. J Med Genet. 1987. PMID: 2443701 Free PMC article.

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