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Date: 1993
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/186928
Description: The Schinzel-Giedion syndrome is a rare autosomal recessive condition with typical facies, skeletal manifestations and congenital hydronephrosis. We report an infant with characteristic findings who h ... More
Reviewed: Reviewed
Date: 1993
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/186932
Description: A phenotypically female infant with 46-XY chromosomes was found to have Smith-Lemli-Opitz syndrome, type II a rare congenital malformation syndrome with many features of the more common classic Smith- ... More
Reviewed: Reviewed
Date: 1991
Language: eng
Resource Type: journal article
Identifier: http://hdl.handle.net/1959.14/186923
Description: Osteodysplastic primordial dwarfism, type II manifests typical skeletal features which have not previously been described in the radiographic literature. We present an infant with characteristic findi ... More
Reviewed: Reviewed
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