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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
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

Erich Roessler Ping Hu; Juliana Marino; Sungkook Hong; Rachel Hart; Seth Berger; Ariel Martinez; Yu Abe; Paul Kruszka; James W Thomas; James C Mullikin NISC Comparative Sequencing Program; Yupeng Wang; Wendy S. W Wong; John E Niederhuber; Benjamin D Solomon; Antonio Richieri-Costa; Lucilene Arilho Ribeiro Bicudo; Maximilian Muenke

Human Mutation Hoboken v. 39, n. 10, p. 1416-1427, 2018

Hoboken 2018

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Hart, R
  2. NISC Comparative Sequencing Program
  3. Solomon, B
  4. Bicudo, L
  5. Martinez , A

Neste Assunto:

  1. Malformações
  2. Mutação Genética
  3. Holoprosencefalia

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

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