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Human Genetics|October 13, 2000
Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate allelesS Castellví-Bel, M Fernández-Burriel, M Rifé, et al.Human Genetics|September 12, 2000
Effect of nonsense mutations on PTEN mRNA stabilityA M Raizis, M M Ferguson, P M GeorgeHuman Genetics|September 12, 2000
Female fetal cells in maternal blood: use of DNA polymorphisms to prove originO Samura, B Pertl, S Sohda, et al.Human Genetics|September 12, 2000
Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individualsM Granzow, S Popp, M Keller, et al.Human Genetics|September 12, 2000
Microscopic assessment of pronuclear embryos is not definitiveA S Lim, V H Goh, C L Su, et al.Human Genetics|September 12, 2000
Variant detection at the delta opioid receptor (OPRD1) locus and population genetics of a novel variant affecting protein sequenceJ Gelernter, H R KranzlerHuman Genetics|September 12, 2000
Fine-mapping of the type 1 diabetes locus (IDDM4) on chromosome 11q and evaluation of two candidate genes (FADD and GALN) by affected sibpair and linkage-disequilibrium analysesS Eckenrode, M P Marron, R Nicholls, et al.Human Genetics|September 12, 2000
Isolation of a paralog of the Doyne honeycomb retinal dystrophy gene from the multiple retinopathy critical region on 11q13N Katsanis, S Venable, J R Smith, et al.Human Genetics|September 12, 2000
Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patientsM De Castro, J García-Planells, E Monrós, et al.Human Genetics|September 12, 2000
Seven ring (X) chromosomes lacking the XIST locus, six with an unexpectedly mild phenotypeC Turner, N R Dennis, D H Skuse, et al.Pageof 959