Kristin Abbott

Zoekresultaten

• 2023

  The role of TBX18 in congenital heart defects in humans not confirmed

  Engwerda, A., Abbott, K. M., Hitzert, M. M., van Ravenswaaij-Arts, C. M. A. & Kerstjens-Frederikse, W. S., feb.-2023, In: European Journal of Human Genetics. 31, blz. 138–141 4 blz.

  Onderzoeksoutput › Academic › peer review

  Open Access

  Bestand
  9 Downloads (Pure)
• 2019

  Fanconi anaemia presenting as acute myeloid leukaemia and myelodysplastic syndrome in adulthood: a family report on co-occurring FANCC and CHEK2 mutations

  Berger, G., van den Berg, E., Smetsers, S., Leegte, B. K., Sijmons, R. H., Abbott, K. M., Mulder, A. B. & Vellenga, E., mrt.-2019, In: British Journal of Haematology. 184, 6, blz. 1071-1073 3 blz.

  Onderzoeksoutput › Academic › peer review

  Open Access

  Bestand
  4 Citaten (Scopus)

  7 Downloads (Pure)