Fibrochondrogenesis in a 17-week fetus: A case expanding the phenotype

American Journal of Medical Genetics

Volumn 75, Issue 3, 1998, Pages 326-329

  Hunt, Nicholas C A ^a   Vujanić, Gordan M ^a  

^a UNIVERSITY HOSPITAL OF WALES   (United Kingdom)

Author keywords

Fetus; Fibrochondrogenesis; Skeletal dysplasia

Indexed keywords

ARTICLE; BONE DYSPLASIA; CHONDROGENESIS; FETUS; FETUS MALFORMATION; FIBROCHONDROGENESIS; FIBROGENESIS; HUMAN; HUMAN TISSUE; MICROGNATHIA; PHENOTYPE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SHORT LIMBED DWARFISM; TONGUE DISEASE;

ABNORMALITIES, MULTIPLE; BONE AND BONES; DWARFISM; FACE; FEMALE; FEMUR; FIBROBLASTS; HUMANS; MICROGNATHISM; OSTEOCHONDRODYSPLASIAS; PHENOTYPE; PREGNANCY; PRENATAL DIAGNOSIS; SKULL; TONGUE;

EID: 0032559182     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19980123)75:3<326::AID-AJMG20>3.0.CO;2-Q     Document Type: Article

References (5)

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