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References

Kyle Drover edited this page Nov 16, 2021 · 5 revisions
  1. Kinder, S. J. et al. The organizer of the mouse gastrula is composed of a dynamic population of progenitor cells for the axial mesoderm. Development 128, 3623–3634 (2001).
  2. Solomon, B. et al. Analysis of genotype-phenotype correlations in human holoprosencephaly. Am. J. Med. Genet. C. Semin. Med. Genet. 154C, 133–141 (2010).
  3. Barratt, K. S. & Arkell, R. M. ZIC2 in Holoprosencephaly BT - Zic family: Evolution, Development and Disease. in (ed. Aruga, J.) 269–299 (Springer Singapore, 2018). doi:10.1007/978-981-10-7311-3_14.
  4. Orioli, I. M. & Castilla, E. E. Epidemiology of holoprosencephaly: Prevalence and risk factors. Am. J. Med. Genet. Part C Semin. Med. Genet. 154C, 13–21 (2010).
  5. Shiota, K. A life-table analysis of the intrauterine fate of malformed human embryos and fetuses. Birth Defects Res. 113, 623–632 (2021).
  6. Tekendo-Ngongang, C., Muenke, M. & Kruszka, P. Holoprosencephaly Overview. (University of Washington, 2020).
  7. Warr, N. et al. Zic2 -associated holoprosencephaly is caused by a transient defect in the organizer region during gastrulation . Hum. Mol. Genet. 17, 2986–2996 (2008).
  8. Elms, P., Siggers, P., Napper, D., Greenfield, A. & Arkell, R. Zic2 is required for neural crest formation and hindbrain patterning during mouse development. Dev. Biol. 264, 391–406 (2003).
  9. Houtmeyers, R. et al. Zic2 mutation causes holoprosencephaly via disruption of NODAL signalling. Hum. Mol. Genet. 25, 3946–3959 (2016).
  10. Nolan, P. M. et al. A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse. Nat. Genet. 25, 440–443 (2000).
  11. Horner, N. R. et al. LAMA: automated image analysis for the developmental phenotyping of mouse embryos. Development 148 (2021).

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