Identification of TCTE3 as a gene responsible for congenital diaphragmatic hernia using a high-resolution single-nucleotide polymorphism array

Pediatric Surgery International

Volumn 27, Issue 2, 2011, Pages 193-198

  Teshiba, Risa ^a,b   Masumoto, Kouji ^b,c   Esumi, Genshiro ^b   Nagata, Kouji ^b   Kinoshita, Yoshiaki ^b   Tajiri, Tatsuro ^b   Taguchi, Tomoaki ^b   Yamamoto, Ken ^a  

^a KYUSHU UNIVERSITY   (Japan)

^b KYUSHU UNIVERSITY   (Japan)

^c FUKUOKA UNIVERSITY   (Japan)

Author keywords

Congenital diaphragmatic hernia; Copy number variation; Microdeletion; Single nucleotide polymorphism array; TCTE3

Indexed keywords

ARTICLE; CLINICAL ARTICLE; CONGENITAL DIAPHRAGM HERNIA; CONTROLLED STUDY; EXON; GENE; GENE DELETION; GENE IDENTIFICATION; GENE LOCUS; GENE NUMBER; GENETIC VARIABILITY; HUMAN; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TCTE3 GENE;

CYTOPLASMIC DYNEINS; DNA; GENE EXPRESSION REGULATION; GENETIC PREDISPOSITION TO DISEASE; HERNIA, DIAPHRAGMATIC; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 78751646170     PISSN: 01790358     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00383-010-2778-z     Document Type: Article

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