Development of novel noninvasive prenatal testing protocol for whole autosomal recessive disease using picodroplet digital PCR

Scientific Reports

Volumn 6, Issue , 2016, Pages

  Chang, Mun Young ^a   Kim, Ah Reum ^b   Kim, Min Young ^c   Kim, Soyoung ^d   Yoon, Jinsun ^e   Han, Jae Joon ^c   Ahn, Soyeon ^c   Kang, Changsoo ^f   Choi, Byung Yoon ^c,g  

^a Chung Ang University   (South Korea)

^b Seoul National University Hospital   (South Korea)

^c Seoul National University Bundang Hospital   (South Korea)

^d LAS Inc   (South Korea)

^e BioCore Co Ltd   (South Korea)

^f Sungshin Women's University   (South Korea)

^g Seoul National University   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; DFNA3 PROTEIN, HUMAN; DNA; GAP JUNCTION PROTEIN; SLC26A4 PROTEIN, HUMAN;

BLOOD; BLOOD SAMPLING; CHEMISTRY; COMPARATIVE STUDY; DISCRIMINANT ANALYSIS; DNA MUTATIONAL ANALYSIS; DNA SEQUENCE; EMBRYOLOGY; FEMALE; FETOMATERNAL TRANSFUSION; FETUS DISEASE; GENETICS; GENOTYPING TECHNIQUE; HUMAN; ISOLATION AND PURIFICATION; MALE; MOLECULAR DIAGNOSIS; PERCEPTION DEAFNESS; POLYMERASE CHAIN REACTION; PREGNANCY; PRENATAL DIAGNOSIS; PROCEDURES; RECESSIVE GENE; SINGLE NUCLEOTIDE POLYMORPHISM;

BLOOD SPECIMEN COLLECTION; CONNEXINS; DISCRIMINANT ANALYSIS; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; FETAL DISEASES; FETOMATERNAL TRANSFUSION; GENES, RECESSIVE; GENOTYPING TECHNIQUES; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MEMBRANE TRANSPORT PROTEINS; MICROCHEMISTRY; MOLECULAR DIAGNOSTIC TECHNIQUES; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; PREGNANCY; PRENATAL DIAGNOSIS; SEQUENCE ANALYSIS, DNA;

EID: 85002603667     PISSN: None     EISSN: 20452322     Source Type: Journal    
DOI: 10.1038/srep37153     Document Type: Article

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