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Page 1
Molecular studies of trisomy 18.
Fisher JM, Harvey JF, Lindenbaum RH, Boyd PA, Jacobs PA. Fisher JM, et al. Among authors: boyd pa. Am J Hum Genet. 1993 Jun;52(6):1139-44. Am J Hum Genet. 1993. PMID: 8503446 Free PMC article. Review.
Limb abnormalities and chorion villus sampling.
Firth HV, Boyd PA, Chamberlain P, MacKenzie IZ, Lindenbaum RH, Huson SM. Firth HV, et al. Among authors: boyd pa. Lancet. 1991 Jul 6;338(8758):51. doi: 10.1016/0140-6736(91)90036-o. Lancet. 1991. PMID: 1676098 No abstract available.
Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe.
Wellesley D, Dolk H, Boyd PA, Greenlees R, Haeusler M, Nelen V, Garne E, Khoshnood B, Doray B, Rissmann A, Mullaney C, Calzolari E, Bakker M, Salvador J, Addor MC, Draper E, Rankin J, Tucker D. Wellesley D, et al. Among authors: boyd pa. Eur J Hum Genet. 2012 May;20(5):521-6. doi: 10.1038/ejhg.2011.246. Epub 2012 Jan 11. Eur J Hum Genet. 2012. PMID: 22234154 Free PMC article.
Autism, language and communication in children with sex chromosome trisomies.
Bishop DV, Jacobs PA, Lachlan K, Wellesley D, Barnicoat A, Boyd PA, Fryer A, Middlemiss P, Smithson S, Metcalfe K, Shears D, Leggett V, Nation K, Scerif G. Bishop DV, et al. Among authors: boyd pa. Arch Dis Child. 2011 Oct;96(10):954-9. doi: 10.1136/adc.2009.179747. Epub 2010 Jul 23. Arch Dis Child. 2011. PMID: 20656736 Free PMC article.
Clinical and genetic heterogeneity in Meckel syndrome.
Paavola P, Salonen R, Baumer A, Schinzel A, Boyd PA, Gould S, Meusburger H, Tenconi R, Barnicoat A, Winter R, Peltonen L. Paavola P, et al. Among authors: boyd pa. Hum Genet. 1997 Nov;101(1):88-92. doi: 10.1007/s004390050592. Hum Genet. 1997. PMID: 9385376
98 results