Hyland VJ - Search Results

1

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

2

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.

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 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.

5

Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.

Hyland VJ, Fernandez KE, Callen DF, MacKinnon RN, Baker E, Friend K, Sutherland GR. Hyland VJ, et al. Hum Genet. 1989 Aug;83(1):61-6. doi: 10.1007/BF00274150. Hum Genet. 1989. PMID: 2570019

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

A linkage group with FRA16B (the fragile site at 16q22.1).

Mulley JC, Hyland VJ, Fratini A, Bates LJ, Gedeon AK, Sutherland GR. Mulley JC, et al. Among authors: hyland vj. Hum Genet. 1989 May;82(2):131-3. doi: 10.1007/BF00284044. Hum Genet. 1989. PMID: 2722188

8

Restriction fragment length polymorphisms detected by anonymous DNA probes mapped to defined intervals of human chromosome 16.

Hyland VJ, Grist S, Sutherland GR. Hyland VJ, et al. Hum Genet. 1988 Jul;79(3):277-9. doi: 10.1007/BF00366251. Hum Genet. 1988. PMID: 2900214

9

Interleukin 4 is at 5q31 and interleukin 6 is at 7p15.

Sutherland GR, Baker E, Callen DF, Hyland VJ, Wong G, Clark S, Jones SS, Eglinton LK, Shannon MF, Lopez AF, et al. Sutherland GR, et al. Among authors: hyland vj. Hum Genet. 1988 Aug;79(4):335-7. doi: 10.1007/BF00282171. Hum Genet. 1988. PMID: 3261707

10

5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia.

Sutherland GR, Baker E, Callen DF, Hyland VJ, May BK, Bawden MJ, Healy HM, Borthwick IA. Sutherland GR, et al. Among authors: hyland vj. Am J Hum Genet. 1988 Sep;43(3):331-5. Am J Hum Genet. 1988. PMID: 3414687 Free PMC article.

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