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American Journal of Medical Genetics|June 28, 1996
Tel Aviv-Heidelberg three-generation offspring study: genetic determinants of plasma fibrinogen levelG Livshits, G Schettler, E Graff, et al.American Journal of Medical Genetics|June 28, 1996
Gonadal (ovarian) dysgenesis in 46,XX individuals: frequency of the autosomal recessive formC M Meyers, J A Boughman, M Rivas, et al.American Journal of Medical Genetics|June 28, 1996
Familial recurrence of tracheoesophageal fistula and associated malformationsK P McMullen, P S Karnes, C R Moir, et al.American Journal of Medical Genetics|June 28, 1996
Confirmation of the Catania brachydactylous type of acrofacial dysostosis: report of a second familyE A Wulfsberg, A B Campbell, I W Lurie, et al.American Journal of Medical Genetics|June 28, 1996
Genetic counseling of isolated carriers of Duchenne muscular dystrophyE P Hoffman, E Pegoraro, P Scacheri, et al.American Journal of Medical Genetics|July 12, 1996
Inheritance of skewed X chromosome inactivation in a large family with an X-linked recessive deafness syndromeK H Orstavik, R E Orstavik, K Eiklid, et al.American Journal of Medical Genetics|July 12, 1996
Linkage analysis in three families with nonspecific X-linked mental retardationS Claes, X X Gu, E Legius, et al.American Journal of Medical Genetics|July 12, 1996
Genetic variation and evolutionary stability of the FMR1 CGG repeat in six closed human populationsE E Eichler, D L NelsonAmerican Journal of Medical Genetics|July 12, 1996
Fragile X founder effects and new mutations in FinlandN Zhong, E Kajanoja, B Smits, et al.American Journal of Medical Genetics|October 23, 1995
Distal deletion of chromosome 13 in a child with the "opitz" GBBB syndromeM Urioste, I Arroyo, A Villa, et al.Pageof 854