Suthers GK - Search Results

1

X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome: localization to Xq12-q21.31 by X inactivation and linkage analysis.

Gibbons RJ, Suthers GK, Wilkie AO, Buckle VJ, Higgs DR. Gibbons RJ, et al. Among authors: suthers gk. Am J Hum Genet. 1992 Nov;51(5):1136-49. Am J Hum Genet. 1992. PMID: 1415255 Free PMC article.

2

High-resolution genetic map around the spinal muscular atrophy (SMA) locus on chromosome 5.

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Buckle VJ, Davies KE. Morrison KE, et al. Among authors: suthers gk. Am J Hum Genet. 1992 Mar;50(3):520-7. Am J Hum Genet. 1992. PMID: 1539593 Free PMC article.

3

Two novel microsatellite markers for prenatal prediction of spinal muscular atrophy (SMA).

Morrison KE, Daniels RJ, Suthers GK, Flynn GA, Francis MJ, Grewal PK, Dennis C, Buckle V, Ignatius J, Dubowitz V, et al. Morrison KE, et al. Among authors: suthers gk. Hum Genet. 1993 Sep;92(2):133-8. doi: 10.1007/BF00219680. Hum Genet. 1993. PMID: 8370578

4

Genetic counseling in rare syndromes: a resampling method for determining an approximate confidence interval for gene location with linkage data from a single pedigree.

Suthers GK, Wilson SR. Suthers GK, et al. Am J Hum Genet. 1990 Jul;47(1):53-61. Am J Hum Genet. 1990. PMID: 2349950 Free PMC article.

5

Genetic mapping of new DNA probes at Xq27 defines a strategy for DNA studies in the fragile X syndrome.

Suthers GK, Mulley JC, Voelckel MA, Dahl N, Väisänen ML, Steinbach P, Glass IA, Schwartz CE, van Oost BA, Thibodeau SN, et al. Suthers GK, et al. Am J Hum Genet. 1991 Mar;48(3):460-7. Am J Hum Genet. 1991. PMID: 1671806 Free PMC article.

6

A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14.

Suthers GK, Turner G, Mulley JC. Suthers GK, et al. Am J Med Genet. 1988 May-Jun;30(1-2):485-91. doi: 10.1002/ajmg.1320300151. Am J Med Genet. 1988. PMID: 3177466

7

Prenatal prediction of spinal muscular atrophy.

Daniels RJ, Suthers GK, Morrison KE, Thomas NH, Francis MJ, Mathew CG, Loughlin S, Heiberg A, Wood D, Dubowitz V, et al. Daniels RJ, et al. Among authors: suthers gk. J Med Genet. 1992 Mar;29(3):165-70. doi: 10.1136/jmg.29.3.165. J Med Genet. 1992. PMID: 1348091 Free PMC article.

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. Among authors: suthers gk. Hum Genet. 1990 Feb;84(3):286-8. doi: 10.1007/BF00200577. Hum Genet. 1990. PMID: 1968038

9

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

10

Four chromosomal breakpoints and four new probes mark out a 10-cM region encompassing the fragile-X locus (FRAXA).

Rousseau F, Vincent A, Rivella S, Heitz D, Triboli C, Maestrini E, Warren ST, Suthers GK, Goodfellow P, Mandel JL, et al. Rousseau F, et al. Among authors: suthers gk. Am J Hum Genet. 1991 Jan;48(1):108-16. Am J Hum Genet. 1991. PMID: 1670748 Free PMC article.

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