Hanson I - Search Results

1

Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations.

Hanson I, Churchill A, Love J, Axton R, Moore T, Clarke M, Meire F, van Heyningen V. Hanson I, et al. Hum Mol Genet. 1999 Feb;8(2):165-72. doi: 10.1093/hmg/8.2.165. Hum Mol Genet. 1999. PMID: 9931324

2

Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly.

Hanson IM, Fletcher JM, Jordan T, Brown A, Taylor D, Adams RJ, Punnett HH, van Heyningen V. Hanson IM, et al. Nat Genet. 1994 Feb;6(2):168-73. doi: 10.1038/ng0294-168. Nat Genet. 1994. PMID: 8162071

3

PAX6 mutations in aniridia.

Hanson IM, Seawright A, Hardman K, Hodgson S, Zaletayev D, Fekete G, van Heyningen V. Hanson IM, et al. Hum Mol Genet. 1993 Jul;2(7):915-20. doi: 10.1093/hmg/2.7.915. Hum Mol Genet. 1993. PMID: 8364574

4

Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations.

Axton RA, Hanson IM, Love J, Seawright A, Prosser J, van Heyningen V. Axton RA, et al. Among authors: hanson im. Mol Cell Probes. 1997 Aug;11(4):287-92. doi: 10.1006/mcpr.1997.0117. Mol Cell Probes. 1997. PMID: 9281415

5

Pax6: more than meets the eye.

Hanson I, Van Heyningen V. Hanson I, et al. Trends Genet. 1995 Jul;11(7):268-72. doi: 10.1016/s0168-9525(00)89073-3. Trends Genet. 1995. PMID: 7482776 Review.

6

A new PAX6 mutation in familial aniridia.

Hanson I, Brown A, van Heyningen V. Hanson I, et al. J Med Genet. 1995 Jun;32(6):488-9. doi: 10.1136/jmg.32.6.488. J Med Genet. 1995. PMID: 7666404 Free PMC article.

7

The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.

Axton R, Hanson I, Danes S, Sellar G, van Heyningen V, Prosser J. Axton R, et al. Among authors: hanson i. J Med Genet. 1997 Apr;34(4):279-86. doi: 10.1136/jmg.34.4.279. J Med Genet. 1997. PMID: 9138149 Free PMC article.

8

A new set of primers for mutation analysis of the human PAX6 gene.

Love J, Axton R, Churchill A, van Heyningen V, Hanson I. Love J, et al. Among authors: hanson i. Hum Mutat. 1998;12(2):128-34. doi: 10.1002/(SICI)1098-1004(1998)12:2<128::AID-HUMU8>3.0.CO;2-N. Hum Mutat. 1998. PMID: 9671274

9

Aniridia.

Hingorani M, Hanson I, van Heyningen V. Hingorani M, et al. Among authors: hanson i. Eur J Hum Genet. 2012 Oct;20(10):1011-7. doi: 10.1038/ejhg.2012.100. Epub 2012 Jun 13. Eur J Hum Genet. 2012. PMID: 22692063 Free PMC article. Review.

10

Inherited PAX6, NF1 and OTX2 mutations in a child with microphthalmia and aniridia.

Henderson RA, Williamson K, Cumming S, Clarke MP, Lynch SA, Hanson IM, FitzPatrick DR, Sisodiya S, van Heyningen V. Henderson RA, et al. Eur J Hum Genet. 2007 Aug;15(8):898-901. doi: 10.1038/sj.ejhg.5201826. Epub 2007 Apr 4. Eur J Hum Genet. 2007. PMID: 17406642

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