van der Ven, A. T., Shril, S., Ityel, H., Vivante, A., Chen, J., Hwang, D., . . . Hildebrandt, F. (2017). Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient with Syndromic CAKUT: A Case Report. Mol Syndromol.
Styl Chicagovan der Ven, Amelie T., et al. "Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient With Syndromic CAKUT: A Case Report." Mol Syndromol 2017.
Citace podle MLAvan der Ven, Amelie T., et al. "Whole-Exome Sequencing Reveals FAT4 Mutations in a Clinically Unrecognizable Patient With Syndromic CAKUT: A Case Report." Mol Syndromol 2017.
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