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Rees Mark I.
Rees M. I.
Rees M.I.
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M.I.
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Mark I.
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http://hub.abes.fr/bmj/periodical/jnnp/2013/volume_84/issue_7/B35A17CA23D45B19E053120B220AE1F6/authorship/5
http://hub.abes.fr/bmj/periodical/thoraxjnl/2006/volume_61/issue_5/B35D6B18C5D1415FE053120B220A9376/authorship/10
http://hub.abes.fr/oup/periodical/hmg/1999/volume_8/issue_9/101093hmg891729/authorship/2
http://hub.abes.fr/oup/periodical/hmg/1994/volume_3/issue_12/101093hmg3122175/authorship/1
http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_10/101093hmgddq063/authorship/13
http://hub.abes.fr/bmj/periodical/jnnp/2010/volume_81/issue_8/B35A17CA1C2A5B19E053120B220AE1F6/authorship/4
http://hub.abes.fr/oup/periodical/hmg/2002/volume_11/issue_7/101093hmg117853/authorship/1
http://hub.abes.fr/oup/periodical/hmg/2010/volume_19/issue_14/101093hmgddq182/authorship/11
http://hub.abes.fr/oup/periodical/qjmedj/2009/volume_102/issue_7/101093qjmedhcp019/authorship/2
http://hub.abes.fr/bmj/periodical/jnnp/2011/volume_83/issue_3/B35A17CA1F3F5B19E053120B220AE1F6/authorship/7
http://hub.abes.fr/bmj/periodical/archdischild/2005/volume_90/issue_5/B3532A3DD6114A1CE053120B220A28C4/authorship/7
http://hub.abes.fr/bmj/periodical/jmg/2001/volume_38/issue_7/B3598D6B5D957CBEE053120B220A90C5/authorship/2
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A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs
Hyperekplexia associated with compound heterozygote mutations in the β-subunit of the human inhibitory glycine receptor (GLRB)
An ovine transgenic Huntington's disease model
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins
Epilepsy genetics: clinical beginnings and social consequences
Evidence for recessive as well as dominant forms of startle disease (hyperekplexia) caused by mutations in the α1 subunit of the inhibitory glycine receptor
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