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American Journal of Medical Genetics|November 11, 1996
Pattern of malformations in the axial skeleton in human trisomy 18 fetusesI Kjaer, J W Keeling, B F HansenAmerican Journal of Medical Genetics|October 27, 1998
Determinants of parental decisions after the prenatal diagnosis of Down syndromeR L Kramer, R K Jarve, Y Yaron, et al.American Journal of Medical Genetics|October 21, 1998
Hereditary febrile seizures: phenotype and evidence for a chromosome 19p locusS L Kugler, E S Stenroos, D E Mandelbaum, et al.American Journal of Medical Genetics|October 21, 1998
Systematic search for uniparental disomy in early fetal losses: the results and a review of the literatureL G Shaffer, C McCaskill, K Adkins, et al.American Journal of Medical Genetics|October 21, 1998
Hearing loss due to the mitochondrial A1555G mutation in Italian familiesR A Casano, Y Bykhovskaya, D F Johnson, et al.American Journal of Medical Genetics|October 22, 1998
Nephrogenic rests and the pathogenesis of Wilms tumor: developmental and clinical considerationsJ B BeckwithAmerican Journal of Medical Genetics|October 22, 1998
Klippel-Trenaunay syndromeS A Berry, C Peterson, W Mize, et al.American Journal of Medical Genetics|October 22, 1998
Congenital heart defects in Sotos syndromeD R Noreau, J Al-Ata, L Jutras, et al.American Journal of Medical Genetics|January 23, 1999
FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndromeM T Abrams, W E Kaufmann, F Rousseau, et al.American Journal of Medical Genetics|January 23, 1999
Deletion of the pseudoautosomal region in a male with a unique Y;13 translocation and short statureA Shanske, J Ellison, P Vuguin, et al.Pageof 854