Williamson R - Search Results

1

Evidence that a locus for familial psoriasis maps to chromosome 4q.

Matthews D, Fry L, Powles A, Weber J, McCarthy M, Fisher E, Davies K, Williamson R. Matthews D, et al. Among authors: williamson r. Nat Genet. 1996 Oct;14(2):231-3. doi: 10.1038/ng1096-231. Nat Genet. 1996. PMID: 8841203

2

Confirmation of genetic heterogeneity in familial psoriasis.

Matthews D, Fry L, Powles A, Weissenbach J, Williamson R. Matthews D, et al. Among authors: williamson r. J Med Genet. 1995 Jul;32(7):546-8. doi: 10.1136/jmg.32.7.546. J Med Genet. 1995. PMID: 7562968 Free PMC article.

3

A human regulatory subunit of type II cAMP-dependent protein kinase localized by its linkage relationship to several cloned chromosome 7q markers.

Wainwright B, Lench N, Davies K, Scambler P, Kruyer H, Williamson R, Jahnsen T, Farrall M. Wainwright B, et al. Among authors: williamson r. Cytogenet Cell Genet. 1987;45(3-4):237-9. doi: 10.1159/000132461. Cytogenet Cell Genet. 1987. PMID: 3691190 No abstract available.

4

Association of the steroid synthesis gene CYP11a with polycystic ovary syndrome and hyperandrogenism.

Gharani N, Waterworth DM, Batty S, White D, Gilling-Smith C, Conway GS, McCarthy M, Franks S, Williamson R. Gharani N, et al. Among authors: williamson r. Hum Mol Genet. 1997 Mar;6(3):397-402. doi: 10.1093/hmg/6.3.397. Hum Mol Genet. 1997. PMID: 9147642

5

Isolation of a polymorphic genomic clone from chromosome 7. Physical and genetic linkage studies to markers around the cystic fibrosis locus.

Davies KA, Lorand L, Waterfield M, Wainwright B, Farrall M, Williamson R. Davies KA, et al. Among authors: williamson r. Hum Genet. 1987 Oct;77(2):122-6. doi: 10.1007/BF00272377. Hum Genet. 1987. PMID: 2888718

6

Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome.

Waterworth DM, Bennett ST, Gharani N, McCarthy MI, Hague S, Batty S, Conway GS, White D, Todd JA, Franks S, Williamson R. Waterworth DM, et al. Among authors: williamson r. Lancet. 1997 Apr 5;349(9057):986-90. doi: 10.1016/S0140-6736(96)08368-7. Lancet. 1997. PMID: 9100625

7

The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease.

Hill ME, Davies KE, Harper P, Williamson R. Hill ME, et al. Among authors: williamson r. Hum Genet. 1982;60(3):222-6. doi: 10.1007/BF00303007. Hum Genet. 1982. PMID: 6286461

8

The genetic basis of polycystic ovary syndrome.

Franks S, Gharani N, Waterworth D, Batty S, White D, Williamson R, McCarthy M. Franks S, et al. Among authors: williamson r. Hum Reprod. 1997 Dec;12(12):2641-8. doi: 10.1093/humrep/12.12.2641. Hum Reprod. 1997. PMID: 9455828 Review.

9

An anonymous clone E9pl (D4S112) localised to 4q26-qter detects an Msp I RFLP.

Robbins TP, Scambler PJ, Davies KE, Williamson R. Robbins TP, et al. Among authors: williamson r. Nucleic Acids Res. 1987 Oct 12;15(19):8122. doi: 10.1093/nar/15.19.8122. Nucleic Acids Res. 1987. PMID: 2444927 Free PMC article.

10

Towards a complete linkage map of the human X chromosome.

Davies KE, Williamson R. Davies KE, et al. Among authors: williamson r. Horiz Biochem Biophys. 1986;8:1-50. Horiz Biochem Biophys. 1986. PMID: 2875929 Review.

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