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American Journal of Medical Genetics|December 31, 1997
Progeroid syndrome with characteristic facial appearance and hand anomalies in father and sonA Giannotti, M C Digilio, R Mingarelli, et al.American Journal of Medical Genetics|December 31, 1997
Birth prevalence, mutation rate, sex ratio, parents' age, and ethnicity in Apert syndromeM M Tolarova, J A Harris, D E Ordway, et al.American Journal of Medical Genetics|December 31, 1997
De novo 16p deletion: ATR-16 syndromeN M Lindor, M G Valdes, M Wick, et al.American Journal of Medical Genetics|December 31, 1997
Velocardiofacial manifestations and microdeletions in schizophrenic inpatientsD Gothelf, A Frisch, H Munitz, et al.American Journal of Medical Genetics|January 31, 1998
Profound biotinidase deficiency in two asymptomatic adultsB Wolf, K Norrgard, R J Pomponio, et al.American Journal of Medical Genetics|January 31, 1998
Esophageal atresia with distal tracheoesophageal fistula in a patient with fronto-metaphyseal dysplasiaP Franceschini, A Guala, D Licata, et al.American Journal of Medical Genetics|January 31, 1998
Dominant inheritance of Kabuki make-up syndromeM Tsukahara, Y Kuroki, K Imaizumi, et al.American Journal of Medical Genetics|January 31, 1998
Prenatal lethality of a homozygous null mutation in the human glucocerebrosidase geneN Tayebi, S R Cushner, W Kleijer, et al.American Journal of Medical Genetics|January 31, 1998
Hand and foot postaxial polydactyly: two different traitsE E Castilla, M da Graca Dutra, R Lugarinho da Fonseca, et al.American Journal of Medical Genetics|January 31, 1998
A gene for FG syndrome maps in the Xq12-q21.31 regionS Briault, R Hill, A Shrimpton, et al.Pageof 854