原发性小头畸形的临床特征及相关基因的研究进展(7)
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[55]Kaindl AM，Passemard S.Many roads lead to primary autosomal recessive microcephaly[J].Prog Neurobiol， 2010，90(3)：363-383.
[56]Karkera JD，Izraeli S，Roessler E，et al.The genomic structure， chromosomal localization， and analysis of SIL as a candidate gene for holoprosencephaly[J].Cytogenet Genome Res，2002，97：62-67.
[57]Aplan PD，Lombardi DP，Ginsberg AM，et al.Disruption of the human SCL locus by "illegitimate" V-(D)-J recombinase activity[J].Science，1990，250：1426-1429.
[58]Pfaff KL，Straub CT，Chiang K，et al.The zebra fish cassiopeia mutant reveals that SIL is required for mitotic spindle organization. Mol Cell Biol，2007，27(16)： 5887-5897.
[59]Collazo-Garcia N，Scherer P，Aplan PD.Cloning and characterization of a murine SIL gene[J].Genomics， 1995，30(3)：506-513.
[60]Izraeli S，Lowe LA，Bertness VL，et al.The SIL gene is required for mouse embryonic axial development and left-right specification[J].Nature，1999，399：691-694.
[收稿日期]2012-07-24 [修回日期]2012-09-14
编辑/李阳利
, 百拇医药(杨仁凯 唐晓军)
[55]Kaindl AM，Passemard S.Many roads lead to primary autosomal recessive microcephaly[J].Prog Neurobiol， 2010，90(3)：363-383.
[56]Karkera JD，Izraeli S，Roessler E，et al.The genomic structure， chromosomal localization， and analysis of SIL as a candidate gene for holoprosencephaly[J].Cytogenet Genome Res，2002，97：62-67.
[57]Aplan PD，Lombardi DP，Ginsberg AM，et al.Disruption of the human SCL locus by "illegitimate" V-(D)-J recombinase activity[J].Science，1990，250：1426-1429.
[58]Pfaff KL，Straub CT，Chiang K，et al.The zebra fish cassiopeia mutant reveals that SIL is required for mitotic spindle organization. Mol Cell Biol，2007，27(16)： 5887-5897.
[59]Collazo-Garcia N，Scherer P，Aplan PD.Cloning and characterization of a murine SIL gene[J].Genomics， 1995，30(3)：506-513.
[60]Izraeli S，Lowe LA，Bertness VL，et al.The SIL gene is required for mouse embryonic axial development and left-right specification[J].Nature，1999，399：691-694.
[收稿日期]2012-07-24 [修回日期]2012-09-14
编辑/李阳利
, 百拇医药(杨仁凯 唐晓军)