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Clinical Genetics|August 1, 1985
An unusual variant chromosome 9 with an extra C-negative, G-dark segment in the short armF S Spedicato, A Di Comite, M Tohidast-AkradClinical Genetics|August 1, 1985
Frequency of fragile X chromosome in normal femalesD Abuelo, K Castree, S Pueschel, et al.Clinical Genetics|November 1, 1979
Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysisA J Vermorken, G T Spierenburg, C A van Bennekom, et al.Clinical Genetics|June 1, 1976
Description of the banding patterns of human chromosomes by acriding orange reverse banding (RFA) and comparison with the Paris banding diagramR S Verma, H A LubsClinical Genetics|October 1, 1994
Molecular and clinical analyses of cystic fibrosis in the south of SpainS Borrego, T Casals, J Dapena, et al.Clinical Genetics|June 1, 1994
Congenital cutis laxa with ligamentous laxity and delayed development, Dandy-Walker malformation and minor heart and osseous defectsA Biver, S De Rijcke, V Toppet, et al.Clinical Genetics|May 1, 1995
18p monosomy with GH-deficiency and empty sella: good response to GH-treatmentE Schober, S Scheibenreiter, H FrischClinical Genetics|May 1, 1995
A small supernumerary marker chromosome X identified by in situ hybridizationA N Silahtaroglu, S Hacihanefioglu, S Yilmaz, et al.Clinical Genetics|June 1, 1995
Problems arising in correlating clinical and molecular data in myotonic dystrophyM Giordano, M S De Angelis, R Cantello, et al.Clinical Genetics|June 1, 1995
Cystic fibrosis mutations and immotile cilia syndromeS Liechti-Gallati, R KraemerPageof 718