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European Journal of Medical Genetics|March 15, 2006
Decreased cholesterol synthesis as a possible aetiological factor in malformations of trisomy 18Wayne W K Lam, J Kirk, N Manning, et al.Human Molecular Genetics|July 1, 1997
Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosisM Tassabehji, K Metcalfe, D Donnai, et al.Personality and Mental Health|September 28, 2016
Measuring child personality when child personality was not measured: Application of a thin-slice approachJennifer L Tackett, Avanté J Smack, Kathrin Herzhoff, et al.Clinical Dysmorphology|January 1, 1995
The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIC)W Reardon, R M Winter, L T Smith, et al.American Journal of Medical Genetics|October 1, 1994
New autosomal dominant form of spondyloepiphyseal dysplasia presenting with atlanto-axial instabilityW Reardon, C M Hall, D G Shaw, et al.American Journal of Human Genetics|September 1, 1996
Linkage analysis of juvenile myoclonic epilepsy and microsatellite loci spanning 61 cM of human chromosome 6p in 19 nuclear pedigrees provides no evidence for a susceptibility locus in this regionF V Elmslie, M P Williamson, M Rees, et al.Journal of Medical Genetics|March 1, 1995
Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further familiesA O Wilkie, S P Yang, D Summers, et al.American Journal of Medical Genetics|August 1, 1992
Five years experience of predictive testing for myotonic dystrophy using linked DNA markersW Reardon, J L Floyd, J Myring, et al.Neuromuscular Disorders : NMD|January 1, 1992
Molecular analysis for the myotonic dystrophy mutation in neuromuscular disordersJ C MacMillan, J Myring, H G Harley, et al.The Journal of Clinical Endocrinology and Metabolism|August 12, 1999
Concurrence of Pendred syndrome, autoimmune thyroiditis, and simple goiter in one familyB Vaidya, R Coffey, B Coyle, et al.Pageof 16