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American Journal of Medical Genetics|February 15, 1993
Genetic counselling in Noonan syndromeM Sharland, M Morgan, G Smith, et al.American Journal of Medical Genetics|February 15, 1993
Mosaicism for deletion 17p11.2 in a boy with the Smith-Magenis syndromeB M Finucane, M B Kurtz, V R Babu, et al.American Journal of Medical Genetics|February 15, 1993
Are the wolffian anomalies in males the phenotype corresponding to the müllerian anomalies in females?J ZlotogoraAmerican Journal of Medical Genetics|February 15, 1993
Skeletal histopathology in fetuses with chondroectodermal dysplasia (Ellis-van Creveld syndrome)F Qureshi, S M Jacques, M I Evans, et al.American Journal of Medical Genetics|January 1, 1993
Hyperphalangism, facial anomalies, hallux valgus, and bronchomalacia: a new syndrome?D Chitayat, S Haj-Chahine, H J Stalker, et al.American Journal of Medical Genetics|January 1, 1993
Absent chondrodysplasia punctata in a male with an Xp terminal deletion involving the putative region for CDPX1 locusT Ogata, P Goodfellow, C Petit, et al.American Journal of Medical Genetics|January 1, 1993
Duplication (20p) in association with thyroid carcinomaP Clark, K L Jones, G R FreidenbergAmerican Journal of Medical Genetics|January 1, 1993
Fetal and neonatal outcome of exposure to anticoagulants during pregnancyV Wong, C H Cheng, K C ChanAmerican Journal of Medical Genetics|January 1, 1993
Characterization of a de novo 48,XX,+r(X),+r(17) by in situ hybridization in a patient with neurofibromatosis (NF1)A Wiktor, D L Van Dyke, L WeissAmerican Journal of Medical Genetics|January 1, 1993
Quantitation of craniofacial anomalies in utero: fetal alcohol and Crouzon syndromes and thanatophoric dysplasiaL F Escobar, D Bixler, L M PadillaPageof 854