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Journal of Medical Genetics|August 1, 1978
Dissociation as probable origin of mosaic 45,XY,t(15;21)/46,XY,i(21q)A M Vianna-Morgante, H G NunesmaiaJournal of Medical Genetics|October 7, 2004
Common variants at the PCOL2 and Sp1 binding sites of the COL1A1 gene and their interactive effect influence bone mineral density in CaucasiansP-Y Liu, Y Lu, J-R Long, et al.Journal of Medical Genetics|October 7, 2004
Genetic polymorphism of CYP1A2 increases the risk of myocardial infarctionM C Cornelis, A El-Sohemy, H CamposJournal of Medical Genetics|February 1, 1978
Popliteal pterygium syndrome: a phenotypic and genetic analysisV Escobar, D WeaverJournal of Medical Genetics|February 1, 1995
Contribution of molecular analyses to the estimation of the risk of congenital myotonic dystrophyA M Cobo, J J Poza, L Martorell, et al.Journal of Medical Genetics|February 1, 1995
Pallister-Hall syndrome and McKusick-Kaufmann syndrome: one entity?K M Unsinn, N Neu, A Krejci, et al.Journal of Medical Genetics|February 1, 1995
DNA methylation based testing of 450 patients suspected of having Prader-Willi syndromeG Gillessen-Kaesbach, S Gross, S Kaya-Westerloh, et al.Journal of Medical Genetics|March 1, 1995
FRAXE and mental retardationJ C Mulley, S Yu, D Z Loesch, 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.Journal of Medical Genetics|March 1, 1995
Heterogeneity in Li-Fraumeni families: p53 mutation analysis and immunohistochemical stainingC MacGeoch, G Turner, L G Bobrow, et al.Pageof 649