Literature DB >> 4461064

Chondrodysplasia punctata (rhizomelic type): case report and pathologic findings.

G I Sugarman.   

Abstract

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Year:  1974        PMID： 4461064

Source DB:  PubMed          Journal:  Birth Defects Orig Artic Ser        ISSN： 0547-6844


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  5 in total

1.  Manifesting heterozygosity in sex-linked spastic paraplegia?

Authors:  I D Young; I F Pye; J R Moore
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-03       Impact factor: 10.154

2.  Hereditary sideroblastic anaemia and ataxia: an X linked recessive disorder.

Authors:  R A Pagon; T D Bird; J C Detter; I Pierce
Journal:  J Med Genet       Date:  1985-08       Impact factor: 6.318

3.  Chondrodysplasia punctata--rhizomelic form. Pathologic and radiologic studies of three infants.

Authors:  E F Gilbert; J M Opitz; J W Spranger; L O Langer; J J Wolfson; C Viseskul
Journal:  Eur J Pediatr       Date:  1976-09-01       Impact factor: 3.183

4.  Morphologic studies in the skeletal dysplasias.

Authors:  D O Sillence; W A Horton; D L Rimoin
Journal:  Am J Pathol       Date:  1979-09       Impact factor: 4.307

5.  Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome.

Authors:  Ryan P Liegel; Adam Ronchetti; D J Sidjanin
Journal:  Mol Genet Metab Rep       Date:  2014
  5 in total

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