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XB-ANAT-506
Papers associated with embryonic structure (and ofd1)
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INTS13 variants causing a recessive developmental ciliopathy disrupt assembly of the Integrator complex., Mascibroda LG., Nat Commun. October 13, 2022; 13 (1): 6054. |
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Left-right patterning in Xenopus conjoined twin embryos requires serotonin signaling and gap junctions., Vandenberg LN., Int J Dev Biol. January 1, 2014; 58 (10-12): 799-809. |
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Loss of nephrocystin-3 function can cause embryonic lethality, Meckel-Gruber-like syndrome, situs inversus, and renal-hepatic-pancreatic dysplasia., Bergmann C., Am J Hum Genet. April 1, 2008; 82 (4): 959-70. |
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