Clinical features of type 2 Stickler syndrome.

Journal of medical genetics

Volumn 41, Issue 8, 2004, Pages

  Poulson, A V ^a   Hooymans, J M ^a   Richards, A J ^a   Bearcroft, P ^a   Murthy, R ^a   Baguley, D M ^a   Scott, J D ^a   Snead, M P ^a  

^a CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 11;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CHONDRODYSPLASIA; CONNECTIVE TISSUE DISEASE; FEMALE; GENETICS; HUMAN; MALE; MIDDLE AGED; MULTIPLE MALFORMATION SYNDROME; MUTATION; PATHOLOGY; PEDIGREE; RETINA DETACHMENT; SYNDROME;

ABNORMALITIES, MULTIPLE; ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; COLLAGEN TYPE XI; CONNECTIVE TISSUE DISEASES; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION; OSTEOCHONDRODYSPLASIAS; PEDIGREE; RETINAL DETACHMENT; SYNDROME;

EID: 16544362845     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2004.018382     Document Type: Article

References (0)