HLXB9 homeobox gene and caudal regression syndrome. (vol 76, pg 205, 2006)

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作者：
Merello, E.
De Marco, P.
Mascelli, S.
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BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY | 2006年 / 76卷 / 07期
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D O I：
10.1002/bdra.20306
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Q [生物科学];
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07 ; 0710 ; 09 ;
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页码：568 / 568
页数：1
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    Merello, E
    De Marco, P
    Mascelli, S
    Raso, A
    Calevo, MG
    Torre, M
    Cama, A
    Lerone, M
    Martucciello, G
    Capra, V
    [J]. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2006, 76 (03): : 205 - 209
  • [2] Involvement of the HLXB9 gene in Currarino Syndrome.
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    Alison J. Ross
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    Yiming Wang
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    Sally A. Lynch
    Susan Lindsay
    Emily Custard
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    [J]. Nature Genetics, 1998, 20 : 358 - 361
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    [J]. Nature Genetics, 1999, 23 (1) : 67 - 70
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    Ludwig Wilkens
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    Daniel Inderbitzin
    Olivier Giger
    Nils von Neuhoff
    [J]. Virchows Archiv, 2011, 458 : 697 - 708
  • [9] Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene (vol 66, pg 1504, 2000)
    Hagan, DM
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    Scambler, P
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (03) : 769 - 769
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