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American Journal of Medical Genetics|January 8, 1999
Expression of the RET proto-oncogene in human embryosT Attié-Bitach, M Abitbol, M Gérard, et al.American Journal of Medical Genetics|December 18, 1998
Long first metacarpal in monozygotic twins with probable Baller-Gerold syndromeP Franceschini, D Licata, A Guala, et al.American Journal of Medical Genetics|December 18, 1998
Renal tubular dysgenesis, absent nipples, and multiple malformations in three brothers: a new, lethal syndromeF M Hisama, M Reyes-Mugica, D S Wargowski, et al.American Journal of Medical Genetics|December 18, 1998
Four novel mutations of the connexin 32 gene in four Japanese families with Charcot-Marie-Tooth disease type 1T Ikegami, C Lin, M Kato, et al.American Journal of Medical Genetics|December 18, 1998
Identification of an unusual marker chromosome by spectral karyotypingB Huang, Y Ning, A N Lamb, et al.American Journal of Medical Genetics|December 18, 1998
Association of terminal chromosome 1 deletion with sertoli cell-only syndromeE H Hathout, K Thompson, M Baum, et al.American Journal of Medical Genetics|December 18, 1998
Germline PTEN mutation in a family with Cowden syndrome and Bannayan-Riley-Ruvalcaba syndromeR T Zori, D J Marsh, G E Graham, et al.American Journal of Medical Genetics|December 18, 1998
Short stature, brachydactyly, nail dysplasia, and mental retardation: further observation of the Tonoki syndromeG Sorge, S Baieli, L Mauceri, et al.American Journal of Medical Genetics|December 8, 1998
Torg osteolysis syndromeD M Eisenstein, A K Poznanski, L M PachmanAmerican Journal of Medical Genetics|December 8, 1998
Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncationJ I Pulai, H Zakeri, P Y Kwok, et al.Pageof 854