2 results for author:"Pantzar T." in Literature citations
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| Acetylcholine receptor pathway mutations explain various fetal akinesia deformation sequence disorders. Michalk A., Stricker S., Becker J., Rupps R., Pantzar T., Miertus J., Botta G., Naretto V.G., Janetzki C., Yaqoob N. et al. Am. J. Hum. Genet. 82:464-476(2008) · UniProtKB (3) · Mapped (23) |
| Renal-hepatic-pancreatic dysplasia: an autosomal recessive condition that is not linked to the PKHD1 gene on chromosome 6p21.1-p12. Schrader K.A., Nelson T.N., McFadden D.E., Pantzar T., Langlois S. Am. J. Med. Genet. A 143A:1806-1808(2007) · Mapped (2) |