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American Journal of Medical Genetics|December 1, 1988
Greig cephalopolysyndactyly syndrome: a possible mouse homologue (Xt-extra toes)R M Winter, S M HusonHuman Genetics|January 1, 1984
Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndromeK E Davies, K Harper, D Bonthron, et al.Human Molecular Genetics|December 1, 1996
Mapping of DFN2 to Xq22J Tyson, S Bellman, V Newton, et al.The New England Journal of Medicine|December 11, 1980
A new genetic basis for hemoglobin-H diseaseL Pressley, D R Higgs, J B Clegg, et al.Journal of Medical Genetics|January 1, 1988
A recognisable short stature syndrome with premature aging and pigmented naeviM Baraitser, J Insley, R M WinterClinical Genetics|July 11, 1998
Internet databases for clinical geneticists--an overviewM A van Steensel, R M WinterJournal of Medical Genetics|December 1, 1985
Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probeM E Pembrey, J M Old, J V Leonard, et al.Human Genetics|December 1, 1990
The major cystic fibrosis mutation in a British populationC J McMahon, S A Genet, H R Middleton-Price, et al.Clinical Dysmorphology|June 3, 2005
Kohlschutter syndrome in siblingsD Donnai, P I Tomlin, R M WinterPageof 23