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Refinado por: Nome da Publicação: Human Mutation remover assunto: Fgf remover
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Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling
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Common genetic causes of holoprosencephaly are limited to a small set of evolutionarily conserved driver genes of midline development coordinated by TGF‐β, hedgehog, and FGF signaling

Roessler, Erich ; Hu, Ping ; Marino, Juliana ; Hong, Sungkook ; Hart, Rachel ; Berger, Seth ; Martinez, Ariel ; Abe, Yu ; Kruszka, Paul ; Thomas, James W. ; Mullikin, James C. ; Wang, Yupeng ; Wong, Wendy S.W. ; Niederhuber, John E. ; Solomon, Benjamin D. ; Richieri‐Costa, Antônio ; Ribeiro‐Bicudo, L.A. ; Muenke, Maximilian

Human mutation, 2018-10, Vol.39 (10), p.1416-1427 [Periódico revisado por pares]

United States: Hindawi Limited

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