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Attributs	Valeurs
type	work Issue
Is Part Of	http://hub.abes.fr/oup/periodical/hmg/1992/volume_1
has manifestation of work	http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_3/m/web http://hub.abes.fr/oup/periodical/hmg/1992/volume_1/issue_3/m/print
Date Copyrighted	1992
Rights	© Oxford University Press
issue	3
is Is Part Of of	Standards for reporting alleles at highly polymorphic loci: a proposal Sequence of the exon-containing regions of the human factor VIII gene A novel mutation in the p53 gene in a Burkitt's lymphoma cell line An Alu variable polyA repeat polymorphism upstream of L-myc at 1p32 cA479 (D3S719): a cosmid mapped telomeric of the Von Hippel Lindau disease gene contains the D3S18 locus Screening for mutations in the open reading frame and promoter of the β-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val→lle Dinucleotide repeat polymorphism at the DXS178 locus Microsatellite polymorphisms at the D11S554 and D11S569 loci Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene Dinucleotide repeat polymorphism at the HOX 2B locus Dinucleotide repeat polymorphism in the Huntington's disease region at the D4S43 locus An X chromosome inactivation assay based on differential methylation of a CpG island coupled to a VNTR polymorphism at the 5′ end of the monoamine oxidase A gene Transcription of deleted mitochondrial DNA in human colon adenocarcinoma cells Characterization of a YAC containing part or all of the Norrie disease locus G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu↑Lys mutation An STS from a cDNA located in the myotonic dystrophy region (DM) on human chromosome 19q13.3 Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci ACE (or PNMT?) in the hole Both mutations in G6PD A — are necessary to produce the G6PD deficient phenotype The PAX3 gene is mapped to human chromosome 2 together with a highly informative CA dinucleotide repeat Dinucleotide repeat polymorphism in the human fibroblast growth factor acidic (FGFA) gene on chromosome 5 The search for Y chromosome polymorphism is extended to negroids Genetic linkage of the human gene for phenylethanol-amine N-methyltransferase (PNMT), the adrenaline-synthesizing enzyme, to DNA markers on chromosome 17q21-q22 Isolation and sequence of two genes associated with a CpG island 5′ of the factor VIII gene Dinucleotide repeat polymorphism at the human erythroid alpha spectrin (SPTA1) locus Author index Cloning of the Huntington disease region in yeast artificial chromosomes A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha l site accounts for a new G6PD deficiency gene in Chinese

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