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American Journal of Medical Genetics|April 1, 1993
Human smooth muscle myosin heavy chain gene mapped to chromosomal region 16q12R Matsuoka, M C Yoshida, Y Furutani, et al.American Journal of Medical Genetics|September 5, 1997
Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndromeE W McPherson, G Laneri, M M Clemens, et al.American Journal of Medical Genetics|September 5, 1997
An apparently acentric marker chromosome originating from 9p with a functional centromere without detectable alpha and beta satellite sequencesG H Vance, C A Curtis, N A Heerema, et al.American Journal of Medical Genetics|September 5, 1997
High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndromeY Y Fang, S Bain, E A Haan, et al.American Journal of Medical Genetics|September 5, 1997
Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18pJ C Wang, L Nemana, S Y Kou, et al.American Journal of Medical Genetics|September 5, 1997
New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19pA Chen, S Wayne, A Bell, et al.American Journal of Medical Genetics|August 22, 1997
Hyperlipidemia, insulin-dependent diabetes mellitus, and rapidly progressive diabetic retinopathy and nephropathy in Prader-Willi syndrome with del(15)(q11.2q13)R Bassali, W H Hoffman, H Chen, et al.American Journal of Medical Genetics|August 22, 1997
Inheritance of familial congenital isolated anorectal malformations: case report and reviewD Landau, J Mordechai, M Karplus, et al.American Journal of Medical Genetics|August 22, 1997
Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1M Caggana, G A Ashley, R J Desnick, et al.American Journal of Medical Genetics|August 22, 1997
Progressive diaphyseal dysplasia: a three-generation family with markedly variable expressivityJ M SaraivaPageof 854