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American Journal of Medical Genetics|June 9, 1999
Presenility of granulocytes in Down syndrome individualsK Yasui, K Shinozaki, T Nakazawa, et al.American Journal of Medical Genetics|August 10, 1999
Congenital cholesteatoma and malformations of the facial nerve: rare manifestations of the BOR syndromeG E Graham, J E AllansonAmerican Journal of Medical Genetics|August 10, 1999
Random X-inactivation in a girl with duplication Xp11.21-p21.3: report of a patient and review of the literatureM Matsuo, K Muroya, K Kosaki, et al.American Journal of Medical Genetics|August 10, 1999
Partial duplication of 4q12q13 leads to a mild phenotypeV Shashi, M N Berry, C Santos, et al.American Journal of Medical Genetics|July 16, 1999
Biochemical variants of Smith-Lemli-Opitz syndromeD W Neklason, K M Andrews, R I Kelley, et al.American Journal of Medical Genetics|July 16, 1999
Case of partial trisomy 2q3 with clinical manifestations of Marshall-Smith syndromeM Z Seidahmed, D E Rooney, M A Salih, et al.American Journal of Medical Genetics|May 14, 1999
Parental origin of the isochromosome 12p in Pallister-Killian syndrome: molecular analysis of one patient and review of the reported casesJ L Struthers, C D Cuthbert, M M KhalifaAmerican Journal of Medical Genetics|May 20, 1999
Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in CaucasiansN Zhong, W Ju, W Xu, et al.American Journal of Medical Genetics|May 20, 1999
Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal populationP C Patsalis, C Sismani, S Stylianou, et al.American Journal of Medical Genetics|May 20, 1999
Search for a Caenorhabditis elegans FMR1 homologue: identification of a new putative RNA-binding protein (PRP-1) that hybridizes to the mouse FMR1 double K homology domainS Shtang, M D Perry, M E PercyPageof 854