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Reforming research assessmentPhenotypic diversity in siblings with partial androgen insensitivity syndromePhysical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28The PLoS community journalsPLoS biology--we're openReplication publicationA simple proposal for the publication of journal citation distributionsLaunching eLife, Part 1.Mutations of the androgen receptor gene identified in perineal hypospadias.Mutational screening of the Wilms's tumour gene, WT1, in males with genital abnormalities.Phenotypic variation and detection of carrier status in the partial androgen insensitivity syndromeAndrogen insensitivity with mental retardation: a contiguous gene syndrome?Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome.MASA syndrome: further clinical delineation and chromosomal localisation.Androgen insensitivity syndrome: a survey of diagnostic procedures and management in the UKMolecular characterization of cell cycle gene CDC7 from Saccharomyces cerevisiae.Differential regulation of the yeast CDC7 gene during mitosis and meiosis.Evidence that xeroderma pigmentosum cells from complementation group E are deficient in a homolog of yeast photolyase.Molecular analysis of muscular dystrophy.Wide variation in androgen receptor dysfunction in complete androgen insensitivity syndrome.Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome.Building a sustainable future for eLifeIs the end in cite?Advancing research.Please welcome our first academic editor-in-chief.Physical mapping of DXS134 close to the DXS52 locus.Rescaling scientific communication.A complex issue.How cells recognize damaged DNA: clues from xeroderma pigmentosum and yeast.How early-career researchers are shaping eLife.A new twist on peer review.Mapping of a cerebellar degeneration related protein and DXS304 around the fragile siteGenetic and physical mapping of a novel region close to the fragile X site on the human X chromosomeBringing eLife to lifeGenetic counselling in complete androgen insensitivity syndrome: trinucleotide repeat polymorphisms, single-strand conformation polymorphism and direct detection of two novel mutations in the androgen receptor genePrenatal diagnosis of androgen insensitivityAndrogen insensitivity syndromeMolecular analysis of the fragile X syndromeFine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosomeMolecular analysis of X-linked diseases
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British researcher, editor and publisher
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Mark Patterson
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Mark Patterson
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مارك باترسون
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