Izvorni znanstveni članak
https://doi.org/10.26800/LV-144-supl7-13
Clinically recognizable disease with negative result of routine gene panel — in search of genetic background with innovative whole genome sequencing
Tea Stipetić
Puni tekst: engleski pdf 658 Kb
str. 13-13
preuzimanja: 113
citiraj
APA 6th Edition
Stipetić, T. (2022). Clinically recognizable disease with negative result of routine gene panel — in search of genetic background with innovative whole genome sequencing. Liječnički vjesnik, 144 (Supp 7), 13-13. https://doi.org/10.26800/LV-144-supl7-13
MLA 8th Edition
Stipetić, Tea. "Clinically recognizable disease with negative result of routine gene panel — in search of genetic background with innovative whole genome sequencing." Liječnički vjesnik, vol. 144, br. Supp 7, 2022, str. 13-13. https://doi.org/10.26800/LV-144-supl7-13. Citirano 16.08.2024.
Chicago 17th Edition
Stipetić, Tea. "Clinically recognizable disease with negative result of routine gene panel — in search of genetic background with innovative whole genome sequencing." Liječnički vjesnik 144, br. Supp 7 (2022): 13-13. https://doi.org/10.26800/LV-144-supl7-13
Harvard
Stipetić, T. (2022). 'Clinically recognizable disease with negative result of routine gene panel — in search of genetic background with innovative whole genome sequencing', Liječnički vjesnik, 144(Supp 7), str. 13-13. https://doi.org/10.26800/LV-144-supl7-13
Vancouver
Stipetić T. Clinically recognizable disease with negative result of routine gene panel — in search of genetic background with innovative whole genome sequencing. Liječnički vjesnik [Internet]. 2022 [pristupljeno 16.08.2024.];144(Supp 7):13-13. https://doi.org/10.26800/LV-144-supl7-13
IEEE
T. Stipetić, "Clinically recognizable disease with negative result of routine gene panel — in search of genetic background with innovative whole genome sequencing", Liječnički vjesnik, vol.144, br. Supp 7, str. 13-13, 2022. [Online]. https://doi.org/10.26800/LV-144-supl7-13
Sažetak
Ključne riječi
CroSeq-GenomeBank, Personalized Medicine, Whole Genome Sequencing
Hrčak ID:
291773
URI
https://hrcak.srce.hr/291773
Datum izdavanja:
28.12.2022.
Posjeta: 334
*