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Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.
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B. ATMIŞ Et Al. , "Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.," 51st Annual ESPN Meeting , vol.33, 2018

ATMIŞ, B. Et Al. 2018. Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.. 51st Annual ESPN Meeting .

ATMIŞ, B., ATMIŞ, A., YARALI, O., ESMERAY ŞENOL, P., & Gemici, A., (2018). Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature. . 51st Annual ESPN Meeting

ATMIŞ, BAHRİYE Et Al. "Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.," 51st Annual ESPN Meeting, 2018

ATMIŞ, BAHRİYE Et Al. "Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.." 51st Annual ESPN Meeting , 2018

ATMIŞ, B. Et Al. (2018) . "Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.." 51st Annual ESPN Meeting .

@conferencepaper{conferencepaper, author={BAHRİYE ATMIŞ Et Al. }, title={Childhood onset nephrotic syndrome with heterozygous mutation in NPHS1 gene: three cases and review of the literature.}, congress name={51st Annual ESPN Meeting}, city={}, country={}, year={2018}}