Literature DB >> 1293391

Rhizomelic chondrodysplasia punctata--a new clinical variant.

R G Gray1, A Green, S Chapman, C McKeown, R B Schutgens, R J Wanders.   

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Year:  1992        PMID： 1293391     DOI： 10.1007/bf01800236

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  3 in total

1.  Antenatal diagnosis of rhizomelic chondrodysplasia punctata in the second trimester.

Authors:  R G Gray; A Green; R B Schutgens; R J Wanders; P A Farndon; C R Kennedy
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  A new type of chondrodysplasia punctata associated with peroxisomal dysfunction.

Authors:  B T Poll-The; P Maroteaux; C Narcy; P Quetin; M Guesnu; R J Wanders; R B Schutgens; J M Saudubray
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

3.  Prenatal diagnosis of inborn errors in peroxisomal beta-oxidation.

Authors:  R J Wanders; R B Schutgens; H van den Bosch; J M Tager; W J Kleijer
Journal:  Prenat Diagn       Date:  1991-04       Impact factor: 3.050
  3 in total

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