Literature DB >> 6147543

First trimester diagnosis of Hunter syndrome on chorionic villi.

W J Kleijer, O P van Diggelen, H C Janse, H Galjaard, Y Dumez, J Boué.   

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Year:  1984        PMID: 6147543     DOI: 10.1016/s0140-6736(84)92952-0

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


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  6 in total

1.  Chorionic villus sampling: diagnostic uses and limitations of enzyme assays.

Authors:  B Fowler; L Giles; A Cooper; I B Sardharwalla
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

2.  Prenatal diagnosis of inherited metabolic disease by chorionic villus analysis: the Edinburgh experience.

Authors:  G T Besley; D M Broadhead
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

3.  The role of cytochemistry in human genetic research.

Authors:  H Galjaard
Journal:  Histochemistry       Date:  1986

4.  Prenatal diagnosis of genetic disease by chorionic villi sampling.

Authors:  I Bartels; I Hansmann
Journal:  Indian J Pediatr       Date:  1986 Jul-Aug       Impact factor: 1.967

Review 5.  Biochemical diagnosis of genetic disease.

Authors:  H Galjaard
Journal:  Experientia       Date:  1986-10-15

6.  Early prenatal investigation of a pregnancy at risk of adenosine deaminase deficiency using chorionic villi.

Authors:  D A Aitken; D H Gilmore; C A Frew; M E Ferguson-Smith; M J Carty; W R Chatfield
Journal:  J Med Genet       Date:  1986-02       Impact factor: 6.318

  6 in total

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