A frameshift mutation in MC4R associated with dominantly inherited
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A frameshift mutation in human MC4R is associated with a dominant form
of obesitypp113 - 114 Christian Vaisse, Karine Clement, Bernard Guy-Grand
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The premature ageing syndrome protein, WRN, is a 3'5'
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Transcription of IAP endogenous retroviruses is constrained by cytosine
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Genetics and insurance in Britain: why more than just the Atlantic divides
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A new logic for DNA engineering using recombination in Escherichia
colipp123 - 128 Youming Zhang, Frank Buchholz, Joep P.P. Muyrers
& A. Francis Stewart doi:10.1038/2417 Abstract|Full text|PDF
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Host response to EBV infection in X-linked lymphoproliferative disease
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NRSF/REST is required in vivo for repression of multiple neuronal
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A gene encoding a transmembrane protein is mutated in patients with diabetes
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Inversin, a novel gene in the vertebrate left-right axis pathway, is
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Mutations in orthologous genes in human spondyloepimetaphyseal dysplasia
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Abnormal maternal behaviour and growth retardation associated with loss
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Mutations in a gene encoding a novel protein tyrosine phosphatase cause
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Evidence for a prostate cancer susceptibility locus on the X chromosome.
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Holoprosencephaly due to mutations in ZIC2, a homologue of
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Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing
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Tumour amplified kinase STK15/BTAK induces centrosome amplification,
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Nonsyndromic hearing impairment is associated with a mutation in
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Behavioural abnormalities and selective neuronal loss in HD transgenic
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Circular chromosome formation in a fission yeast mutant defective in
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5'
exonuclease
