Mulley JC - Search Results

1

Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci.

Kozman HM, Phillips HA, Callen DF, Sutherland GR, Mulley JC. Kozman HM, et al. Among authors: mulley jc. Cytogenet Cell Genet. 1993;62(4):194-8. doi: 10.1159/000133474. Cytogenet Cell Genet. 1993. PMID: 8440136

2

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.

Richards RI, Holman K, Kozman H, Kremer E, Lynch M, Pritchard M, Yu S, Mulley J, Sutherland GR. Richards RI, et al. J Med Genet. 1991 Dec;28(12):818-23. doi: 10.1136/jmg.28.12.818. J Med Genet. 1991. PMID: 1757956 Free PMC article.

3

Linkage between the fragile X and F9, DXS52 (St14), DXS98 (4D-8) and DXS105 (cX55.7).

Mulley J, Turner G, Bain S, Sutherland GR. Mulley J, et al. Am J Med Genet. 1988 May-Jun;30(1-2):567-80. doi: 10.1002/ajmg.1320300158. Am J Med Genet. 1988. PMID: 2902797

4

Identification of a highly polymorphic marker within intron 7 of the ALAS2 gene and suggestion of at least two loci for X-linked sideroblastic anemia.

Cox TC, Kozman HM, Raskind WH, May BK, Mulley JC. Cox TC, et al. Among authors: mulley jc. Hum Mol Genet. 1992 Nov;1(8):639-41. doi: 10.1093/hmg/1.8.639. Hum Mol Genet. 1992. PMID: 1301172

5

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1.

Beggs AH, Phillips HA, Kozman H, Mulley JC, Wilton SD, Kunkel LM, Laing NG. Beggs AH, et al. Among authors: mulley jc. Genomics. 1992 Aug;13(4):1314-5. doi: 10.1016/0888-7543(92)90054-v. Genomics. 1992. PMID: 1505962

6

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: mulley jc. Genomics. 1991 Nov;11(3):756-9. doi: 10.1016/0888-7543(91)90085-s. Genomics. 1991. PMID: 1685482

7

Diagnostic molecular genetics of the fragile X.

Sutherland GR, Mulley JC. Sutherland GR, et al. Among authors: mulley jc. Clin Genet. 1990 Jan;37(1):2-11. doi: 10.1111/j.1399-0004.1990.tb03383.x. Clin Genet. 1990. PMID: 1967989 Review.

8

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: mulley jc. Am J Hum Genet. 1991 Jun;48(6):1051-7. Am J Hum Genet. 1991. PMID: 2035525 Free PMC article.

9

Localisation of human PGP and HAGH genes to 16p13.3.

Mulley JC, Barton N, Callen DF. Mulley JC, et al. Cytogenet Cell Genet. 1990;53(2-3):175-6. doi: 10.1159/000132923. Cytogenet Cell Genet. 1990. PMID: 2164460

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: mulley jc. 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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