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Incidence of Smith-Lemli-Opitz syndrome in Ontario, Canada.
Nowaczyk MJ, McCaughey D, Whelan DT, Porter FD. Nowaczyk MJ, et al. Among authors: whelan dt. Am J Med Genet. 2001 Jul 22;102(1):18-20. doi: 10.1002/1096-8628(20010722)102:1<18::aid-ajmg1376>3.0.co;2-e. Am J Med Genet. 2001. PMID: 11471166
Pregnancy in a healthy woman with untreated citrullinemia.
Potter MA, Zeesman S, Brennan B, Kobayashi K, Gao HZ, Tabata A, Saheki T, Whelan DT. Potter MA, et al. Among authors: whelan dt. Am J Med Genet A. 2004 Aug 15;129A(1):77-82. doi: 10.1002/ajmg.a.20559. Am J Med Genet A. 2004. PMID: 15266621
Paternal transmission of fragile X syndrome.
Zeesman S, Zwaigenbaum L, Whelan DT, Hagerman RJ, Tassone F, Taylor SA. Zeesman S, et al. Among authors: whelan dt. Am J Med Genet A. 2004 Aug 30;129A(2):184-9. doi: 10.1002/ajmg.a.30191. Am J Med Genet A. 2004. PMID: 15316964
Risk reversals in predictive testing for Huntington disease.
Almqvist E, Adam S, Bloch M, Fuller A, Welch P, Eisenberg D, Whelan D, Macgregor D, Meschino W, Hayden MR. Almqvist E, et al. Am J Hum Genet. 1997 Oct;61(4):945-52. doi: 10.1086/514873. Am J Hum Genet. 1997. PMID: 9382108 Free PMC article.
37 results