Callen DF - 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. Among authors: callen df. Hum Genet. 1990 Feb;84(3):286-8. doi: 10.1007/BF00200577. Hum Genet. 1990. PMID: 1968038

2

Four dinucleotide repeat polymorphisms on human chromosome 16 at D16S289, D16S318, D16S319 and D16S320.

Shen Y, Thompson AT, Holman K, Callen DF, Sutherland GR, Richards RI. Shen Y, et al. Among authors: callen df. Hum Mol Genet. 1992 Dec;1(9):773. doi: 10.1093/hmg/1.9.773. Hum Mol Genet. 1992. PMID: 1302615 No abstract available.

3

The gene for the human IgA Fc receptor maps to 19q13.4.

Kremer EJ, Kalatzis V, Baker E, Callen DF, Sutherland GR, Maliszewski CR. Kremer EJ, et al. Among authors: callen df. Hum Genet. 1992 Apr;89(1):107-8. doi: 10.1007/BF00207054. Hum Genet. 1992. PMID: 1577457 No abstract available.

4

Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1.

Kozman HM, Gedeon AK, Whitmore S, Suthers GK, Callen DF, Sutherland GR, Mulley JC. Kozman HM, et al. Among authors: callen df. Genomics. 1991 Nov;11(3):756-9. doi: 10.1016/0888-7543(91)90085-s. Genomics. 1991. PMID: 1685482

5

Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome.

Wilson PJ, Suthers GK, Callen DF, Baker E, Nelson PV, Cooper A, Wraith JE, Sutherland GR, Morris CP, Hopwood JJ. Wilson PJ, et al. Among authors: callen df. Hum Genet. 1991 Mar;86(5):505-8. doi: 10.1007/BF00194643. Hum Genet. 1991. PMID: 1901826

6

Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).

Breuning MH, Snijdewint FG, Brunner H, Verwest A, Ijdo JW, Saris JJ, Dauwerse JG, Blonden L, Keith T, Callen DF, et al. Breuning MH, et al. Among authors: callen df. J Med Genet. 1990 Oct;27(10):603-13. doi: 10.1136/jmg.27.10.603. J Med Genet. 1990. PMID: 1978860 Free PMC article.

7

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: callen df. Am J Hum Genet. 1990 Aug;47(2):187-95. Am J Hum Genet. 1990. PMID: 2378346 Free PMC article.

8

Molecular genetics of human chromosome 16.

Sutherland GR, Reeders S, Hyland VJ, Callen DF, Fratini A, Mulley JC. Sutherland GR, et al. Among authors: callen df. 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.

9

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. Among authors: callen df. Hum Genet. 1989 Aug;83(1):61-6. doi: 10.1007/BF00274150. Hum Genet. 1989. PMID: 2570019

10

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. Genomics. 1989 Apr;4(3):348-54. doi: 10.1016/0888-7543(89)90341-8. Genomics. 1989. PMID: 2714795

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