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Fetal exposure to DES results in de-regulation of Wnt7a during uterine
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Differential SMN2 expression associated with SMA severitypp230 - 231 Dimitar K. Gavrilov, Xiangyang Shi, Kamna Das, T. Conrad Gilliam
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DRPLA aggregation and transglutaminase, revisitedp231 Laszlo Lorand doi:10.1038/3033 Full text|PDF
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The Fanconi anaemia group G gene FANCG is identical with XRCC9pp281 - 283 Johan P. de Winter, Quinten Waisfisz, Martin A. Rooimans, Carola G.M. van Berkel, Lucine Bosnoyan-Collins, Noa Alon, Madeleine Carreau, Olaf Bender, Ilja Demuth, Detlev Schindler, Jan C. Pronk, Fré Arwert, Holger Hoehn, Martin Digweed, Manuel Buchwald
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A Pro12Ala substitution in PPAR2 associated with decreased receptor
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Rapid amplification of a retrotransposon subfamily is evolving the mouse
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Impaired glucose tolerance in mice with a targeted impairment of insulin
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Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic
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A genome-wide scan for human obesity genes reveals a major susceptibility
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Esx1 is an X-chromosome-imprinted regulator of placental development
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Assignment of Tangier disease to chromosome 9q31 by a graphical linkage
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Inversin, a novel gene in the vertebrate left-right axis pathway, is
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