Branchio-oto (BO) syndrome and oculo-auriculo-vertebral phenotype: Overlapping clinical findings in a child from a BO family

Clinical Genetics

Volumn 49, Issue 6, 1996, Pages 300-302

  Sensi, A ^a,d   Cocchi, G ^b   Martini, A ^c   Garani, G ^c   Trevisi, P ^c   Calzolari, E ^a  

^a UNIVERSITY HOSPITAL OF FERRARA   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c UNIVERSITY OF FERRARA   (Italy)

^d Dipto di Med Sperim e Diagnostica   (Italy)

Author keywords

Branchio oto syndrome; Branchio oto renal syndrome; Oculo auriculo vertebral spectrum

Indexed keywords

ARTICLE; BRANCHIOOTO SYNDROME; BRANCHIOOTORENAL SYNDROME; CASE REPORT; CONGENITAL MALFORMATION; CRANIAL NERVE PARALYSIS; EPICANTHUS; FAMILY STUDY; FEMALE; GENETIC COUNSELING; GOLDENHAR SYNDROME; GROWTH RETARDATION; HUMAN; HYPERTELORISM; INFANT; LONG PHILTRUM; MACROSTOMIA; MANDIBLE HYPOPLASIA; MICROGNATHIA; PHENOTYPE; PRIORITY JOURNAL; VERTEBRA MALFORMATION;

EID: 0029818705     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb03792.x     Document Type: Article

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