Sillence DO - Search Results

1

Fibrochondrogenesis in male twins at 24 weeks gestation.

Bankier A, Fortune D, Duke J, Sillence DO. Bankier A, et al. Among authors: sillence do. Am J Med Genet. 1991 Jan;38(1):95-8. doi: 10.1002/ajmg.1320380121. Am J Med Genet. 1991. PMID: 2012139

2

Medical complications of achondroplasia: a multicentre patient review.

Hunter AG, Bankier A, Rogers JG, Sillence D, Scott CI Jr. Hunter AG, et al. J Med Genet. 1998 Sep;35(9):705-12. doi: 10.1136/jmg.35.9.705. J Med Genet. 1998. PMID: 9733026 Free PMC article. Review.

3

Distinct skeletal abnormalities in four girls with Shprintzen-Goldberg syndrome.

Adès LC, Morris LL, Power RG, Wilson M, Haan EA, Bateman JF, Milewicz DM, Sillence DO. Adès LC, et al. Among authors: sillence do. Am J Med Genet. 1995 Jul 17;57(4):565-72. doi: 10.1002/ajmg.1320570410. Am J Med Genet. 1995. PMID: 7573130 Review.

4

Familial Scheuermann disease: a genetic and linkage study.

McKenzie L, Sillence D. McKenzie L, et al. J Med Genet. 1992 Jan;29(1):41-5. doi: 10.1136/jmg.29.1.41. J Med Genet. 1992. PMID: 1552543 Free PMC article.

5

Desbuquois syndrome complicated by obstructive sleep apnoea and cervical kyphosis.

Ogle RF, Wilson MJ, Kozlowski K, Sillence DO. Ogle RF, et al. Among authors: sillence do. Am J Med Genet. 1994 Jul 1;51(3):216-21. doi: 10.1002/ajmg.1320510308. Am J Med Genet. 1994. PMID: 8074147

6

Congenital synspondylism.

Wiles CR, Taylor TF, Sillence DO. Wiles CR, et al. Among authors: sillence do. Am J Med Genet. 1992 Feb 1;42(3):288-95. doi: 10.1002/ajmg.1320420305. Am J Med Genet. 1992. PMID: 1536163

7

Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctata.

Sheffield LJ, Osborn AH, Hutchison WM, Sillence DO, Forrest SM, White SJ, Dahl HH. Sheffield LJ, et al. Among authors: sillence do. J Med Genet. 1998 Dec;35(12):1004-8. doi: 10.1136/jmg.35.12.1004. J Med Genet. 1998. PMID: 9863597 Free PMC article.

8

X linked mental retardation with non-deletional alpha thalassaemia (ATR-X): further delineation of the phenotype.

Ogle R, DeSouza M, Cunningham C, Kerr B, Sillence D. Ogle R, et al. J Med Genet. 1994 Mar;31(3):245-7. doi: 10.1136/jmg.31.3.245. J Med Genet. 1994. PMID: 8014976 Free PMC article.

9

The Wolf-Hirschhorn syndrome in adulthood: evaluation of a 24-year-old man with a rec(4) chromosome.

Ogle R, Sillence DO, Merrick A, Ell J, Lo B, Robson L, Smith A. Ogle R, et al. Among authors: sillence do. Am J Med Genet. 1996 Oct 16;65(2):124-7. doi: 10.1002/(SICI)1096-8628(19961016)65:2<124::AID-AJMG8>3.0.CO;2-S. Am J Med Genet. 1996. PMID: 8911603

10

Natural history of blue sclerae in osteogenesis imperfecta.

Sillence D, Butler B, Latham M, Barlow K. Sillence D, et al. Am J Med Genet. 1993 Jan 15;45(2):183-6. doi: 10.1002/ajmg.1320450207. Am J Med Genet. 1993. PMID: 8456800

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