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American Journal of Medical Genetics|January 10, 1997
VACTERL with hydrocephalus in twins due to Fanconi anemia (FA): mutation in the FAC geneP M Cox, R A Gibson, N Morgan, et al.American Journal of Medical Genetics|March 17, 1997
Severe liver impairment in a cystic fibrosis-affected child homozygous for the G542X mutationG Castaldo, E Rippa, D Salvatore, et al.American Journal of Medical Genetics|March 17, 1997
Premature aging syndrome with osteosarcoma, cataracts, diabetes mellitus, osteoporosis, erythroid macrocytosis, severe growth and developmental deficiencyN Okamoto, K Satomura, Y Hatsukawa, et al.American Journal of Medical Genetics|March 17, 1997
PCR and FISH analysis of a ring Y chromosomeO Henegariu, S Kernek, M A Keating, et al.American Journal of Medical Genetics|March 17, 1997
Presence of hemoglobinopathies in Sicily: a historic perspectiveG Schilirò, E Mirabile, R Testa, et al.American Journal of Medical Genetics|May 16, 1997
Familial hydronephrosis unlinked to the HLA complexA Santavá, A Utíkalová, A Bártová, et al.American Journal of Medical Genetics|May 16, 1997
VACTERL-hydrocephaly, DK-phocomelia, and cerebro-cardio-radio-reno-rectal communityI W Lurie, C FerenczAmerican Journal of Medical Genetics|May 16, 1997
A case of presumptive monosomy 21 re-diagnosed as unbalanced t(5p;21q) by FISH and review of literatureM A Iqbal, M Z Ahmed, D Wu, et al.American Journal of Medical Genetics|April 18, 1997
Isolation of chromosome 18-specific brain transcripts as positional candidates for bipolar disorderT Yoshikawa, A R Sanders, L E Esterling, et al.American Journal of Medical Genetics|April 18, 1997
Lack of association between juvenile myoclonic epilepsy and GABRA5 and GABRB3 genesM Guipponi, P Thomas, C Girard-Reydet, et al.Pageof 854