The molecular basis of human congenital limb malformations.
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Biased Polyphenism in Polydactylous Cats Carrying a Single Point Mutation: The Hemingway Model for Digit NoveltyRole of Genetic Factors in the Pathogenesis of Radial Deficiencies in Humans.Conserved cis-regulatory regions in a large genomic landscape control SHH and BMP-regulated Gremlin1 expression in mouse limb buds.Dinosaurs, Chameleons, Humans, and Evo-Devo Path: Linking Étienne Geoffroy's Teratology, Waddington's Homeorhesis, Alberch's Logic of "Monsters," and Goldschmidt Hopeful "Monsters".The two domain hypothesis of limb prepattern and its relevance to congenital limb anomalies.Tibial hemimelia associated with GLI3 truncation.Characterization of a novel fusion gene EML4-NTRK3 in a case of recurrent congenital fibrosarcoma.Defective Hand1 phosphoregulation uncovers essential roles for Hand1 in limb morphogenesis.Genetic basis of congenital upper limb anomalies: analysis of 487 cases of a specialized clinic.Genetic vulnerabilities to prenatal alcohol exposure: Limb defects in sonic hedgehog and GLI2 heterozygous mice.Thalidomide Embryopathy: An Enigmatic ChallengeQuantification of gene expression patterns to reveal the origins of abnormal morphogenesis
P2860
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P2860
The molecular basis of human congenital limb malformations.
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
The molecular basis of human congenital limb malformations.
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type
label
The molecular basis of human congenital limb malformations.
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prefLabel
The molecular basis of human congenital limb malformations.
@en
P2860
P356
P1476
The molecular basis of human congenital limb malformations.
@en
P2093
Simone Probst
P2860
P304
P356
10.1002/WDEV.59
P577
2012-04-26T00:00:00Z