drs. Y.J. Vos

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E-mail:
y.j.vos umcg.nl

Research

  1. 2003
  2. Kariola, R., Otway, R., Lonnqvist, KE., Raevaara, TE., Macrae, F., Vos, YJ., Kohonen-Corish, M., Hofstra, RMW., & Nystrom-Lahti, M. (2003). Two mismatch repair gene mutations found in a colon cancer patient - which one is pathogenic? HUMAN GENETICS, 112(2), 105-109. https://doi.org/10.1007/s00439-002-0866-4
  3. Criado, GR., Aytes, AP., Martinez, F., Vos, YJ., Verlind, E., Lopez, AGM., Sanchez, IGD., & Schrander-Stumpel, C. (2003). X-linked hydrocephalus: Another two families with an L1 mutation. Genetic counseling, 14(1), 57-65.
  4. 2002
  5. Raevaara, TE., Timohariu, T., Lonnqvist, KE., Kariola, R., Steinhoff, M., Hofstra, RMW., Mangold, E., Vos, YJ., & Nystrom-Lahti, M. (2002). Description and functional analysis of a novel in frame mutation linked to hereditary non-polyposis colorectal cancer. JOURNAL OF MEDICAL GENETICS, 39(10), 747-750.
  6. Sztriha, L., Vos, YJ., Verlind, E., Johansen, J., & Berg, B. (2002). X-linked hydrocephalus: A novel missense mutation in the L1CAM gene. Pediatric neurology, 27(4), 293-296. [PII S0887-8994(02)00440-X].
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