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Clinical Genetics|August 1, 1994
Adults with Williams-Beuren syndrome: evaluation of the medical, psychological and behavioral aspectsL Plissart, M Borghgraef, P Volcke, et al.Clinical Genetics|September 1, 1994
A 12-year preventive program for beta-thalassemia in Northern SardiniaM Longinotti, P Pistidda, L Oggiano, et al.Clinical Genetics|September 1, 1994
Exclusion of linkage to 14q23-24 in a family with Holt-Oram syndromeJ C Ruiz, E Legius, H Cuppens, et al.Clinical Genetics|September 1, 1994
Congenital cardiac defect in a patient with mosaic 45,X/46,XX,i(21q) karyotypeM C Digilio, R Mingarelli, B Marino, et al.Clinical Genetics|September 1, 1994
A case of de novo interstitial deletion of chromosome 9(p12p13)J C Giltay, K B Gerssen-Schoorl, A van der WagenClinical Genetics|October 1, 1994
Marfan and cri du chat syndromes in an 18-month-old child: evidence of phenotype interactionM W McClellan, W L Golden, W G WilsonClinical Genetics|April 1, 1976
beta-Galactosidase deficiency in an adult: a biochemical and somatic cell genetic study on a variant of GM1-gangliosidosisJ F Koster, M F Niermeijer, M C Loonen, et al.Clinical Genetics|October 1, 1993
A family with autosomal dominant polycystic kidney disease not linked to chromosome 16p13.3S Jeffery, A K Saggar-Malik, S Morgan, et al.Clinical Genetics|October 1, 1993
Mosaic trisomy 16 in a thriving infant: maternal heterodisomy for chromosome 16N M Lindor, S M Jalal, S N Thibodeau, et al.Clinical Genetics|October 1, 1993
The Myhre syndrome: report of two casesD García-Cruz, L E Figuera, A Feria-Velazco, et al.Pageof 718