Fowles L - Search Results

1

De novo mutations of the Patched gene in nevoid basal cell carcinoma syndrome help to define the clinical phenotype.

Wicking C, Gillies S, Smyth I, Shanley S, Fowles L, Ratcliffe J, Wainwright B, Chenevix-Trench G. Wicking C, et al. Among authors: fowles l. Am J Med Genet. 1997 Dec 19;73(3):304-7. Am J Med Genet. 1997. PMID: 9415689

2

Genomic screen for genes involved in mammalian craniofacial development.

Fowles LF, Bennetts JS, Berkman JL, Williams E, Koopman P, Teasdale RD, Wicking C. Fowles LF, et al. Genesis. 2003 Feb;35(2):73-87. doi: 10.1002/gene.10165. Genesis. 2003. PMID: 12533789

3

The PCNA-associated factor KIAA0101/p15(PAF) binds the potential tumor suppressor product p33ING1b.

Simpson F, Lammerts van Bueren K, Butterfield N, Bennetts JS, Bowles J, Adolphe C, Simms LA, Young J, Walsh MD, Leggett B, Fowles LF, Wicking C. Simpson F, et al. Exp Cell Res. 2006 Jan 1;312(1):73-85. doi: 10.1016/j.yexcr.2005.09.020. Epub 2005 Nov 8. Exp Cell Res. 2006. PMID: 16288740

4

Evolutionary conservation and murine embryonic expression of the gene encoding the SERTA domain-containing protein CDCA4 (HEPP).

Bennetts JS, Fowles LF, Berkman JL, van Bueren KL, Richman JM, Simpson F, Wicking C. Bennetts JS, et al. Among authors: fowles lf. Gene. 2006 Jun 7;374:153-65. doi: 10.1016/j.gene.2006.01.027. Epub 2006 Mar 20. Gene. 2006. PMID: 16546331

5

Identification and analysis of novel genes expressed in the mouse embryonic facial primordia.

Bennetts JS, Fowles LF, Butterfield NC, Berkman JL, Teasdale RD, Simpson F, Wicking C. Bennetts JS, et al. Among authors: fowles lf. Front Biosci. 2006 Sep 1;11:2631-46. doi: 10.2741/1997. Front Biosci. 2006. PMID: 16720340

6

Murine embryonic expression of the gene for the UV-responsive protein p15(PAF).

van Bueren KL, Bennetts JS, Fowles LF, Berkman JL, Simpson F, Wicking C. van Bueren KL, et al. Among authors: fowles lf. Gene Expr Patterns. 2007 Jan;7(1-2):47-50. doi: 10.1016/j.modgep.2006.05.006. Epub 2006 May 25. Gene Expr Patterns. 2007. PMID: 16815099

7

Parental experiences of ultrarapid genomic testing for their critically unwell infants and children.

Brett GR, Martyn M, Lynch F, de Silva MG, Ayres S, Gallacher L, Boggs K, Baxendale A, Schenscher S, King-Smith S, Fowles L, Springer A, Lunke S, Vasudevan A, Krzesinski E, Pinner J, Sandaradura SA, Barnett C, Patel C, Wilson M, Stark Z. Brett GR, et al. Among authors: fowles l. Genet Med. 2020 Dec;22(12):1976-1985. doi: 10.1038/s41436-020-0912-4. Epub 2020 Jul 28. Genet Med. 2020. PMID: 32719395 Free article.

8

Queensland Consumers' Awareness and Understanding of Clinical Genetics Services.

Wallingford CK, Cutler K, Istiko SN, Fowles LF, Lamb R, Bean J, Healy L, Hondow G, Pratt G, Vidgen ME, Waddell N, Evans E, Bunker D, McInerney-Leo AM. Wallingford CK, et al. Among authors: fowles lf. Front Genet. 2020 Oct 15;11:537743. doi: 10.3389/fgene.2020.537743. eCollection 2020. Front Genet. 2020. PMID: 33193608 Free PMC article.

9

Attitudes of Australian dermatologists on the use of genetic testing: A cross-sectional survey with a focus on melanoma.

Primiero CA, Baker AM, Wallingford CK, Maas EJ, Yanes T, Fowles L, Janda M, Young MA, Nisselle A, Terrill B, Lodge JM, Tiller JM, Lacaze P, Andersen H, McErlean G, Turbitt E, Soyer HP, McInerney-Leo AM. Primiero CA, et al. Among authors: fowles l. Front Genet. 2022 Oct 24;13:919134. doi: 10.3389/fgene.2022.919134. eCollection 2022. Front Genet. 2022. PMID: 36353112 Free PMC article.

10

Evaluation of a Genetics Education Program for Health Interpreters: A Pilot Study.

Vidgen ME, Fowles LF, Istiko SN, Evans E, Cutler K, Sullivan K, Bean J, Healy L, Hondow G, McInerney-Leo AM, Pratt G, Robins D, Best S, Finlay K, Ramarao-Milne P, Waddell N. Vidgen ME, et al. Among authors: fowles lf. Front Genet. 2022 Feb 3;12:771892. doi: 10.3389/fgene.2021.771892. eCollection 2021. Front Genet. 2022. PMID: 35186003 Free PMC article.

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