Torthaí cuardaigh - Barber, John C. K. 

Comments on important genetic topics from papers in other journals: The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene i... de réir Barber, John C K

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Medical genetics: advances in brief: Diagnosis of genetic disease using recombinant DNA. Third edition de réir Barber, John C K

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Medical genetics: advances in brief: Epidermolysis bullosa simplex: evidence in two families for keratin gene abnormalities de réir Barber, John C K

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Medical genetics: advances in brief: Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene de réir Barber, John C K

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Medical genetics: advances in brief de réir Barber, John C K

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Medical genetics: advances in brief: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumours de réir Barber, John C K

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Medical genetics: advances in brief: Identification of a second pseudo-autosomal region near the Xq and Yq telomeres de réir Barber, John C K

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Medical genetics: advances in brief: Complete characterization of a large marker chromosome by reverse and forward chromosome painting de réir Barber, John C K

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Medical genetics: advances in brief: Duplication in the hypoxanthine phosphoribosyl-transferase gene caused by Alu-Alu recombination in a patient with Lesch-Nyhan syndrome de réir Barber, John C K

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Medical genetics: advances in brief: Medical genetics: advances in brief de réir Barber, John C K

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Medical genetics: advances in brief: Identification of the von Hippel-Lindau disease tumour suppressor gene de réir Barber, John C K

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Medical genetics: advances in brief: Amyotrophic lateral sclerosis and structural defects in Cu, Zn superoxide dismutase de réir Barber, John C K

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Medical genetics: advances in brief: Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci de réir Barber, John C K

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Medical genetics: advances in brief: Diagnosis of human genetic disease using recombinant DNA; fourth edition de réir Barber, John C K

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Medical genetics: advances in brief de réir Barber, John C K

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Medical genetics: advances in brief: SRVX, a sex reversing locus in Xp21.2→p22.11 de réir Barber, John C K

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Medical genetics: advances in brief de réir Barber, John C K

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Medical genetics: advances in brief: Localization of the achondroplasia gene to the distal 2-5 Mb of human chromosome 4p de réir Barber, John C K

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Medical genetics: advances in brief de réir Barber, John C K

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Medical genetics: advances in brief: Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation de réir Barber, John C K

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