Wake SA - Search Results

1

Alerting genetic relatives to a risk of serious inherited disease without a patient's consent.

Suthers GK, McCusker EA, Wake SA. Suthers GK, et al. Among authors: wake sa. Med J Aust. 2011 Apr 18;194(8):385-6. doi: 10.5694/j.1326-5377.2011.tb03026.x. Med J Aust. 2011. PMID: 21495936 No abstract available.

2

Doctors breaching patient privacy: Orwell redux.

Suthers GK, McCusker EA, Wake SA. Suthers GK, et al. Among authors: wake sa. Med J Aust. 2011 Jun 20;194(12):670. doi: 10.5694/j.1326-5377.2011.tb03169.x. Med J Aust. 2011. PMID: 21692736 No abstract available.

3

Dissemination of genetic risk information to relatives in the fragile X syndrome: guidelines for genetic counselors.

McConkie-Rosell A, Robinson H, Wake S, Staley LW, Heller K, Cronister A. McConkie-Rosell A, et al. Am J Med Genet. 1995 Dec 4;59(4):426-30. doi: 10.1002/ajmg.1320590406. Am J Med Genet. 1995. PMID: 8585560

4

Cystic fibrosis carrier screening in two New South Wales country towns.

Wake SA, Rogers CJ, Colley PW, Hieatt EA, Jenner CF, Turner GM. Wake SA, et al. Med J Aust. 1996 Apr 15;164(8):471-4. doi: 10.5694/j.1326-5377.1996.tb122123.x. Med J Aust. 1996. PMID: 8614337

5

Analysis of DNA probes for the prenatal diagnosis of cystic fibrosis.

Dry PJ, Wake S, Robertson CF, Colley P, Sheffield LJ. Dry PJ, et al. Med J Aust. 1989 Aug 7;151(3):131, 133-6. Med J Aust. 1989. PMID: 2569157

6

Prevalence of fragile X syndrome.

Turner G, Webb T, Wake S, Robinson H. Turner G, et al. Am J Med Genet. 1996 Jul 12;64(1):196-7. doi: 10.1002/(SICI)1096-8628(19960712)64:1<196::AID-AJMG35>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826475

7

Counselling risk figures for fragile X carrier females of varying band sizes for use in predicting the likelihood of retardation in their offspring.

Turner AM, Robinson H, Wake S, Laing SJ, Leigh D, Turner G. Turner AM, et al. Am J Med Genet. 1994 Jul 15;51(4):458-62. doi: 10.1002/ajmg.1320510432. Am J Med Genet. 1994. PMID: 7943019

8

Informed choice in fragile X syndrome and its effects on prevalence.

Robinson H, Wake S, Wright F, Laing S, Turner G. Robinson H, et al. Am J Med Genet. 1996 Jul 12;64(1):198-202. doi: 10.1002/(SICI)1096-8628(19960712)64:1<198::AID-AJMG36>3.0.CO;2-G. Am J Med Genet. 1996. PMID: 8826476

9

Dizygous twinning and premature menopause in fragile X syndrome.

Turner G, Robinson H, Wake S, Martin N. Turner G, et al. Lancet. 1994 Nov 26;344(8935):1500. doi: 10.1016/s0140-6736(94)90313-1. Lancet. 1994. PMID: 7968130 No abstract available.

10

Case finding for the fragile X syndrome and its consequences.

Turner G, Robinson H, Wake S, Laing S, Partington M. Turner G, et al. BMJ. 1997 Nov 8;315(7117):1223-6. doi: 10.1136/bmj.315.7117.1223. BMJ. 1997. PMID: 9393231 Free PMC article. No abstract available.

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