Schmid type metaphyseal chondrodysplasia [4]

Indian Pediatrics

Volumn 42, Issue 12, 2005, Pages 1252-

  Gokhale, Sankalp ^a   Mehta, Sunil ^a  

^a Rajhans Hospital   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; AUTOSOMAL DOMINANT INHERITANCE; BONE MATURATION; CASE REPORT; CHONDRODYSPLASIA; CLINICAL FEATURE; FEMALE; FEMUR EPIPHYSIS; GENE MUTATION; HUMAN; LETTER; METAPHYSIS; SCHMID TYPE METAPHYSEAL CHONDRODYSPLASIA; VAGINAL DELIVERY;

ADOLESCENT; FEMALE; HUMANS; OSTEOCHONDRODYSPLASIAS;

EID: 32644443762     PISSN: 00196061     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (3)

1. Wynne-Davies R, Hall M, Apley AG. Atlas of Skeletal Dysplasia. Edinburgh: Churchill Livingstone 1985; p. 131.
2. Lachman RS, Rimoin DL, Spranger J. Metaphyseal chondrodysplasia, Schmid type. Clinical and radiographic delineation with a review of the literature. Pediatr Radiol 1988; 18: 93-102.
3. Matthew L. Warman I, Abbott M, Apte SS. A type X collagen mutation causes Schmid metaphyseal chondrodysplasia Nature Genetics 1993; 5: 79-82.