Familial occurrence of oculoauriculovertebral dysplasia and Franceschetti syndrome;Familiare Haufung von okuloaurikulovertebraler Dysplasie und Franceschetti-Syndrom

HNO

Volumn 44, Issue 8, 1996, Pages 452-455

  Bestelmeyer, U ^a   Weerda, H ^a   Siegert, R ^a   Greiwe, M ^a   Schwinger, E ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

Author keywords

Franceschetti syndrome; oculoauriculovertebral dysplasia; recurrence risk

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; EAR DYSPLASIA; FAMILIAL DISEASE; HUMAN; MAJOR CLINICAL STUDY; MANDIBULOFACIAL DYSOSTOSIS; RECURRENT DISEASE; RISK ASSESSMENT; CHILD; CONGENITAL MALFORMATION; EXTERNAL EAR; FEMALE; GENETIC SCREENING; GENETICS; GOLDENHAR SYNDROME; HETEROZYGOTE DETECTION; MALE; PRESCHOOL CHILD; RISK FACTOR;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; EAR, EXTERNAL; FEMALE; GENETIC SCREENING; GOLDENHAR SYNDROME; HETEROZYGOTE DETECTION; HUMANS; MALE; RISK FACTORS;

EID: 0029778226     PISSN: 00176192     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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