Detection of monogenic disorders by microarray

被引：0

作者：

Capkova, Pavlina ^{[1
,2
]}

Curtisova, Vaclava ^{[2
,3
]}

Spurna, Zuzana ^{[2
,3
]}

Stefekova, Andrea ^{[1
]}

Srovnal, Josef ^{[4
]}

Stellmachova, Julia ^{[1
]}

Punova, Lucia ^{[1
]}

Petrkova, Jana ^{[1
]}

Mracka, Enkhjargalan ^{[1
]}

Duchoslavova, Jana ^{[2
,3
]}

Travnickova, Sarka ^{[2
,3
]}

Vrtel, Radek ^{[1
,2
]}

机构：

[1] Univ Hosp Olomouc, Dept Med Genet, Olomouc, Czech Republic

[2] Palacky Univ Olomouc, Fac Med & Dent, Dept Med Genet, Olomouc, Czech Republic

[3] Univ Hosp Olomouc, Dept Med Genet, Olomouc, Czech Republic

[4] Palacky Univ Olomouc, Inst Mol & Translat Med, Fac Med & Dent, Olomouc, Czech Republic

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

P12.001.A

引用

页码：526 / 526

页数：1

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