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注意：仅列出部分参考文献，下载原文获取全部文献信息。Variant type and position predict two distinct limb phenotypes in patients with GLI3-mediated polydactyly syndromes
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Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
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Shivakumar Vasanth et al.
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Momoko Maekawa et al.
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Katarina Dathe et al.
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Brachy-Syndactyly caused by loss of Sfrp2 function
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M Moser et al.
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Tbx5 and Tbx4 trigger limb initiation through activation of the Wnt/Fgf signaling cascade
JK Takeuchi et al.
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Developmental mechanisms underlying polydactyly in the mouse mutant Doublefoot
AP Crick et al.
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Identification of Glis1, a novel Gli-related, Kruppel-like zinc finger protein containing transactivation and repressor functions
YS Kim et al.
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A high-resolution genetic, physical, and comparative gene map of the doublefoot (Dbf) region of mouse chromosome 1 and the region of conserved synteny on human chromosome 2q35
C Hayes et al.
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Physical and functional interactions between Zic and Gli proteins
Y Koyabu et al.
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A Daluiski et al.
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