Disruption of teashirt zinc finger homeobox 1 is associated with congenital aural atresia in humans

American Journal of Human Genetics

Volumn 89, Issue 6, 2011, Pages 813-819

  Feenstra, Ilse ^a   Vissers, Lisenka E L M ^a,b   Pennings, Ronald J E ^a,c   Nillessen, Willy ^a   Pfundt, Rolph ^a   Kunst, Henricus P ^a,c   Admiraal, Ronald J ^a,c   Veltman, Joris A ^a,b   Van Ravenswaaij Arts, Conny M A ^d   Brunner, Han G ^a,b   Cremers, Cor W R J ^a,c  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^c RADBOUD UNIVERSITY   (Netherlands)

^d UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 18Q; CHROMOSOME DELETION; CONGENITAL AURAL ATRESIA; CONGENITAL MALFORMATION; FEMALE; GENE; GENE DISRUPTION; GENE MUTATION; HEMIZYGOSITY; HUMAN; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD; SEQUENCE ANALYSIS; TSHZ1 GENE;

ABNORMALITIES, MULTIPLE; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 18; EAR CANAL; FEMALE; FOOT DEFORMITIES, CONGENITAL; GENETIC ASSOCIATION STUDIES; HAPLOINSUFFICIENCY; HEARING LOSS; HOMEODOMAIN PROTEINS; HUMANS; INFANT; MALE; PEDIGREE; PREGNANCY; TOMOGRAPHY, X-RAY COMPUTED; ULTRASONOGRAPHY, PRENATAL;

EID: 83455188207     PISSN: 00029297     EISSN: 15376605     Source Type: Journal    
DOI: 10.1016/j.ajhg.2011.11.008     Document Type: Article

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