Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia

Journal of Medical Genetics

Volumn 48, Issue 5, 2011, Pages 299-307

  Wat, Margaret J ^a   Veenma, Danielle ^b   Hogue, Jacob ^c   Holder, Ashley M ^d   Yu, Zhiyin ^a   Wat, Jeanette J ^e   Hanchard, Neil ^a   Shchelochkov, Oleg A ^f   Fernandes, Caraciolo J ^a   Johnson, Anthony ^a   Lally, Kevin P ^g   Slavotinek, Anne ^c   Danhaive, Olivier ^h   Schaible, Thomas ⁱ   Cheung, Sau Wai ^a   Rauen, Katherine A ^c   Tonk, Vijay S ^j   Tibboel, Dick ^b   de Klein, Annelies ^b   Scott, Daryl A ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b ERASMUS MEDICAL CENTER   (Netherlands)

^c UNIVERSITY OF CALIFORNIA   (United States)

^d WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e RICE UNIVERSITY   (United States)

^f UNIVERSITY OF IOWA HOSPITALS AND CLINICS   (United States)

^g UNIVERSITY OF TEXAS MEDICAL SCHOOL   (United States)

^h BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

ⁱ UNIVERSITY OF HEIDELBERG   (Germany)

^j TEXAS TECH UNIVERSITY HEALTH SCIENCES CENTER SCHOOL OF MEDICINE   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 16P; CHROMOSOME 1Q; CLINICAL ARTICLE; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DIAPHRAGM; DIAPHRAGM HERNIA; GENE DELETION; HUMAN; MUTATION; PENTALOGY OF CANTRELL; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID SUBSTITUTION; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 11; CHROMOSOMES, HUMAN, PAIR 16; CHROMOSOMES, HUMAN, PAIR 17; CHROMOSOMES, HUMAN, PAIR 8; COMPARATIVE GENOMIC HYBRIDIZATION; DIAPHRAGMATIC EVENTRATION; DNA-BINDING PROTEINS; FEMALE; GENOME, HUMAN; HERNIA, DIAPHRAGMATIC; HUMANS; INFANT; INFANT, NEWBORN; MALE; MUTATION; TRANSCRIPTION FACTORS;

EID: 79955542031     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2011.089680     Document Type: Article

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