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Deletion and duplication: unusual case of diagnostics for patient with cystic fibrosis. / Deryabina, S.; Lagutina, O.; Nikolaeva, E. et al.
In: European Journal of Human Genetics, Vol. 28, No. SUPPL 1, 12.2020, p. 210-210.

Research output: Contribution to journal › Meeting Abstract › peer-review

Harvard

Deryabina, S, Lagutina, O, Nikolaeva, E & Nikitina, NE 2020, 'Deletion and duplication: unusual case of diagnostics for patient with cystic fibrosis', European Journal of Human Genetics, vol. 28, no. SUPPL 1, pp. 210-210.

APA

Deryabina, S., Lagutina, O., Nikolaeva, E., & Nikitina, N. E. (2020). Deletion and duplication: unusual case of diagnostics for patient with cystic fibrosis. European Journal of Human Genetics, 28(SUPPL 1), 210-210.

Vancouver

Deryabina S, Lagutina O, Nikolaeva E, Nikitina NE. Deletion and duplication: unusual case of diagnostics for patient with cystic fibrosis. European Journal of Human Genetics. 2020 Dec;28(SUPPL 1):210-210.

Author

Deryabina, S. ; Lagutina, O. ; Nikolaeva, E. et al. / Deletion and duplication: unusual case of diagnostics for patient with cystic fibrosis. In: European Journal of Human Genetics. 2020 ; Vol. 28, No. SUPPL 1. pp. 210-210.

BibTeX

@article{13792e95c10648829a46a6e0aa55168f,
title = "Deletion and duplication: unusual case of diagnostics for patient with cystic fibrosis",
author = "S. Deryabina and O. Lagutina and E. Nikolaeva and Nikitina, {N. E.}",
year = "2020",
month = dec,
language = "English",
volume = "28",
pages = "210--210",
journal = "European Journal of Human Genetics",
issn = "1018-4813",
publisher = "Nature Publishing Group",
number = "SUPPL 1",

}

RIS

TY - JOUR

T1 - Deletion and duplication: unusual case of diagnostics for patient with cystic fibrosis

AU - Deryabina, S.

AU - Lagutina, O.

AU - Nikolaeva, E.

AU - Nikitina, N. E.

PY - 2020/12

Y1 - 2020/12

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000598482600389

M3 - Meeting Abstract

VL - 28

SP - 210

EP - 210

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

SN - 1018-4813

IS - SUPPL 1

ER -

ID: 20521669