Apparently new osteodysplastic and primordial short stature with severe microdontia, opalescent teeth, and rootless molars in two siblings

American Journal of Medical Genetics

Volumn 111, Issue 4, 2002, Pages 420-428

  Kantaputra, Piranit N ^a  

^a CHIANG MAI UNIVERSITY   (Thailand)

Author keywords

Dentinogenesis imperfecta; Large nose; Microcephaly; Microdontia; Opalescent teeth; Osteodysplasia; Primordial dwarfism; Rootless teeth; Seckel syndrome

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BONE DYSPLASIA; CASE REPORT; EAR MALFORMATION; FEMALE; GROWTH RETARDATION; HUMAN; INTRAUTERINE GROWTH RETARDATION; MALE; MALFORMATION SYNDROME; MOLAR TOOTH; NOSE MALFORMATION; PIGMENT DISORDER; PRIORITY JOURNAL; SHORT STATURE; SIBLING; TOE MALFORMATION; TOOTH MALFORMATION; BONE; CONGENITAL MALFORMATION; DWARFISM; GENETICS; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY;

ABNORMALITIES, MULTIPLE; ADOLESCENT; BONE AND BONES; CASE REPORT; DWARFISM; FEMALE; HUMAN; MALE; SUPPORT, NON-U.S. GOV'T; TOOTH ABNORMALITIES; HUMANS;

TRAPEZIUM; TURCICA;

EID: 0036707802     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10589     Document Type: Article

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