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Connection

Benjamin Fogelgren to Abnormalities, Multiple

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This is a "connection" page, showing publications Benjamin Fogelgren has written about Abnormalities, Multiple.
Benjamin Fogelgren
Connection Strength
0.353
Abnormalities, Multiple
  1. Fogelgren B, Kuroyama MC, McBratney-Owen B, Spence AA, Malahn LE, Anawati MK, Cabatbat C, Alarcon VB, Marikawa Y, Lozanoff S. Misexpression of Six2 is associated with heritable frontonasal dysplasia and renal hypoplasia in 3H1 Br mice. Dev Dyn. 2008 Jul; 237(7):1767-79.
    View in: PubMed
    Score: 0.319
  2. Seixas C, Choi SY, Polgar N, Umberger NL, East MP, Zuo X, Moreiras H, Ghossoub R, Benmerah A, Kahn RA, Fogelgren B, Caspary T, Lipschutz JH, Barral DC. Arl13b and the exocyst interact synergistically in ciliogenesis. Mol Biol Cell. 2016 Jan 15; 27(2):308-20.
    View in: PubMed
    Score: 0.033
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