Sutherland GR - Search Results

1

Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE.

Gedeon AK, Meinänen M, Adès LC, Kääriäinen H, Gécz J, Baker E, Sutherland GR, Mulley JC. Gedeon AK, et al. Among authors: sutherland gr. Am J Hum Genet. 1995 Apr;56(4):907-14. Am J Hum Genet. 1995. PMID: 7536393 Free PMC article.

2

Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.

Callen DF, Mulley JC, Baker EG, Sutherland GR. Callen DF, et al. Among authors: sutherland gr. Hum Genet. 1987 Nov;77(3):236-40. doi: 10.1007/BF00284476. Hum Genet. 1987. PMID: 3479386

3

Genotype-phenotype relationships in fragile X syndrome: a family study.

Loesch DZ, Huggins R, Hay DA, Gedeon AK, Mulley JC, Sutherland GR. Loesch DZ, et al. Among authors: sutherland gr. Am J Hum Genet. 1993 Nov;53(5):1064-73. Am J Hum Genet. 1993. PMID: 8213832 Free PMC article.

4

Integrating maps of chromosome 16.

Mulley JC, Sutherland GR. Mulley JC, et al. Among authors: sutherland gr. Curr Opin Genet Dev. 1993 Jun;3(3):425-31. doi: 10.1016/0959-437x(93)90116-7. Curr Opin Genet Dev. 1993. PMID: 8353417 Review.

5

Incidence and origin of "null" alleles in the (AC)n microsatellite markers.

Callen DF, Thompson AD, Shen Y, Phillips HA, Richards RI, Mulley JC, Sutherland GR. Callen DF, et al. Among authors: sutherland gr. Am J Hum Genet. 1993 May;52(5):922-7. Am J Hum Genet. 1993. PMID: 8488841 Free PMC article.

6

Identification of the gene FMR2, associated with FRAXE mental retardation.

Gecz J, Gedeon AK, Sutherland GR, Mulley JC. Gecz J, et al. Among authors: sutherland gr. Nat Genet. 1996 May;13(1):105-8. doi: 10.1038/ng0596-105. Nat Genet. 1996. PMID: 8673085

7

Fragile X syndrome and fragile XE mental retardation.

Sutherland GR, Mulley JC. Sutherland GR, et al. Prenat Diagn. 1996 Dec;16(13):1199-211. doi: 10.1002/(SICI)1097-0223(199612)16:13<1199::AID-PD95>3.0.CO;2-T. Prenat Diagn. 1996. PMID: 9061751 Review.

8

FMR2 expression in families with FRAXE mental retardation.

Gécz J, Oostra BA, Hockey A, Carbonell P, Turner G, Haan EA, Sutherland GR, Mulley JC. Gécz J, et al. Among authors: sutherland gr. Hum Mol Genet. 1997 Mar;6(3):435-41. doi: 10.1093/hmg/6.3.435. Hum Mol Genet. 1997. PMID: 9147647

9

Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient.

Gecz J, Baker E, Donnelly A, Ming JE, McDonald-McGinn DM, Spinner NB, Zackai EH, Sutherland GR, Mulley JC. Gecz J, et al. Among authors: sutherland gr. Hum Genet. 1999 Jan;104(1):56-63. doi: 10.1007/s004390050910. Hum Genet. 1999. PMID: 10071193

10

The clinical significance of fragile sites on human chromosomes.

Sutherland GR, Baker E. Sutherland GR, et al. Clin Genet. 2000 Sep;58(3):157-61. doi: 10.1034/j.1399-0004.2000.580301.x. Clin Genet. 2000. PMID: 11076037 Review.

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