Literature DB >> 2122105

Antenatal diagnosis of rhizomelic chondrodysplasia punctata in the second trimester.

R G Gray1, A Green, R B Schutgens, R J Wanders, P A Farndon, C R Kennedy.   

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Year:  1990        PMID： 2122105     DOI： 10.1007/bf01799400

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


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  4 in total

Review 1.  Prenatal and perinatal diagnosis of peroxisomal disorders.

Authors:  R B Schutgens; G Schrakamp; R J Wanders; H S Heymans; J M Tager; H van den Bosch
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

2.  Prenatal diagnosis of rhizomelic chondrodysplasia punctata.

Authors:  S Hoefler; G Hoefler; A B Moser; P A Watkins; W W Chen; H W Moser
Journal:  Prenat Diagn       Date:  1988-10       Impact factor: 3.050

3.  Heterogeneity of Chondrodysplasia punctata.

Authors:  J W Spranger; J M Opitz; U Bidder
Journal:  Humangenetik       Date:  1971

4.  Simple diagnosis of the Zellweger syndrome by gas-liquid chromatography of dimethylacetals.

Authors:  I Björkhem; L Sisfontes; B Boström; B F Kase; R Blomstrand
Journal:  J Lipid Res       Date:  1986-07       Impact factor: 5.922
  4 in total
  1 in total

1.  Rhizomelic chondrodysplasia punctata--a new clinical variant.

Authors:  R G Gray; A Green; S Chapman; C McKeown; R B Schutgens; R J Wanders
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
  1 in total

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