Clinical identification of a human equivalent to the short ear (se) murine phenotype

Annales de Genetique

Volumn 37, Issue 4, 1994, Pages 184-191

  Lacombe, D ^a   Toutain, A ^a   Gorlin, R J ^a   Oley, C A ^a   Battin, J ^a  

^a HÔPITAL PELLEGRIN   (France)

Author keywords

bone morphogenetic protein; EPS syndrome; microtia; short ear murine mutation; skeletal dysplasia

Indexed keywords

BONE MORPHOGENETIC PROTEIN;

ARTICLE; BONE DYSPLASIA; CHILD; CLINICAL ARTICLE; EAR DYSPLASIA; EAR MALFORMATION; HUMAN; MALFORMATION SYNDROME; MICROTIA; MOUSE; MUTANT; NONHUMAN; PATELLA; SEQUENCE HOMOLOGY; SHORT STATURE;

ANIMAL; BODY HEIGHT; CASE REPORT; CHILD, PRESCHOOL; CHROMOSOME MAPPING; COMPARATIVE STUDY; CRYPTORCHIDISM; EAR, EXTERNAL; FEMALE; HUMAN; INFANT; MALE; MICE; MICROGNATHISM; MUTATION; PATELLA; PHENOTYPE; SYNDROME;

EID: 0028610388     PISSN: 00033995     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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