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American Journal of Medical Genetics|November 1, 1992
Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndromeM R Altherr, J F Gusella, J J Wasmuth, et al.American Journal of Medical Genetics|November 1, 1992
Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplicationG A Nicholson, M L Kennerson, B J Keats, et al.American Journal of Medical Genetics|November 1, 1992
Update on a family with hand-foot-genital syndrome: hypospadias and urinary tract abnormalities in two boys from the fourth generationA E Donnenfeld, D S Schrager, S L CorsonAmerican Journal of Medical Genetics|November 1, 1992
Parental sex effect in spina bifida: a role for genomic imprinting?S Chatkupt, P R Lucek, M R Koenigsberger, et al.American Journal of Medical Genetics|June 1, 1992
New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher diseaseV M Pratt, J A Trofatter, M B Larsen, et al.American Journal of Medical Genetics|February 15, 1992
Molecular study of 45,X conceptuses: correlation with clinical findingsI Lorda-Sanchez, F Binkert, M Maechler, et al.American Journal of Medical Genetics|July 1, 1992
Bilateral anophthalmia, esophageal atresia, and right cryptorchidism: a new entity?I Arroyo, M J García, C E Cimadevilla, et al.American Journal of Medical Genetics|April 1, 1992
Linkage and risk assessment in fragile X families using new DNA probes at Xq27N J Carpenter, J Swartz-Boyd, J K Prichard, et al.American Journal of Medical Genetics|September 1, 1992
DNA-testing for Huntington's disease in The Netherlands: a retrospective study on psychosocial effectsA Tibben, M Vegter-van der Vlis, M I Skraastad, et al.American Journal of Medical Genetics|July 15, 1992
Autosomal recessive acrorenal syndromeM Miltényi, A E Czeizel, L Balogh, et al.Pageof 854