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American Journal of Medical Genetics|January 1, 1993
Apparent Greig cephalopolysyndactyly and sinus node diseaseJ P Fryns, P De Waele, L Van der Hauwaert, et al.American Journal of Medical Genetics|January 1, 1993
Pericentric inversion of chromosome 4 giving rise to dup(4p) and dup(4q) recombinants within a single kindredB Hirsch, S BaldingerAmerican Journal of Medical Genetics|January 1, 1993
Congenital defects of lower limbs and associated malformations: a population based studyU G Froster, P A BairdAmerican Journal of Medical Genetics|January 1, 1993
Stable inheritance of the CMT1A DNA duplication in two patients with CMT1 and NF1J R Lupski, L Pentao, L L Williams, et al.American Journal of Medical Genetics|August 1, 1993
Hypertrichosis, atrophic skin, ectropion, and macrostomia (Barber-Say syndrome): report of a new caseS Martínez Santana, F Pérez Alvarez, J L Frías, et al.American Journal of Medical Genetics|August 1, 1993
Further delineation of the epidermal nevus syndrome: two cases with new findings and literature reviewT A Grebe, M E Rimsza, S F Richter, et al.American Journal of Medical Genetics|August 1, 1993
Cerebro-reno-digital (Meckel-like) syndrome with Dandy-Walker malformation, cystic kidneys, hepatic fibrosis, and polydactylyM Genuardi, C Dionisi-Vici, G Sabetta, et al.American Journal of Medical Genetics|August 1, 1993
Chorioretinal dysplasia-microcephaly-mental retardation syndrome: report of an American familyL S Sadler, L K RobinsonAmerican Journal of Medical Genetics|August 1, 1993
Of monsters and prodigies: the interpretation of birth defects in the sixteenth centuryM T Walton, R M Fineman, P J WaltonAmerican Journal of Medical Genetics|August 1, 1993
Norman-Roberts syndrome: clinical and molecular studiesP Iannetti, C E Schwartz, J Dietz-Band, et al.Pageof 854