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Asymptomatic maternal myasthenia as a cause of the Pena-Shokeir phenotype.
Brueton LA, Huson SM, Cox PM, Shirley I, Thompson EM, Barnes PR, Price J, Newsom-Davis J, Vincent A. Brueton LA, et al. Am J Med Genet. 2000 May 1;92(1):1-6. doi: 10.1002/(sici)1096-8628(20000501)92:1<1::aid-ajmg1>3.0.co;2-h. Am J Med Genet. 2000. PMID: 10797415
Six cases of 7p deletion: clinical, cytogenetic, and molecular studies.
Chotai KA, Brueton LA, van Herwerden L, Garrett C, Hinkel GK, Schinzel A, Mueller RF, Speleman F, Winter RM. Chotai KA, et al. Among authors: brueton la. Am J Med Genet. 1994 Jul 1;51(3):270-6. doi: 10.1002/ajmg.1320510320. Am J Med Genet. 1994. PMID: 7521123 Review.
Craniodiaphyseal dysplasia.
Brueton LA, Winter RM. Brueton LA, et al. J Med Genet. 1990 Nov;27(11):701-6. doi: 10.1136/jmg.27.11.701. J Med Genet. 1990. PMID: 2277386 Free PMC article. Review. No abstract available.
Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.
Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Goodman FR, et al. Among authors: brueton la. Am J Hum Genet. 2000 Jul;67(1):197-202. doi: 10.1086/302961. Epub 2000 Jun 5. Am J Hum Genet. 2000. PMID: 10839976 Free PMC article.
79 results