Literature DB >> 2512420

A survey on prenatal diagnosis of inherited metabolic diseases in Japan.

K Tada1, J Aikawa, Y Igarashi, K Hayasaka, K Narisawa, M Owada, T Kitagawa.   

Abstract

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Year:  1989        PMID： 2512420     DOI： 10.1007/bf03335392

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


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  3 in total

Review 1.  Non-ketotic hyperglycinaemia: clinical and biochemical aspects.

Authors:  K Tada; K Hayasaka
Journal:  Eur J Pediatr       Date:  1987-05       Impact factor: 3.183

2.  Feasibility of prenatal diagnosis of nonketotic hyperglycinemia: existence of the glycine cleavage system in placenta.

Authors:  K Hayasaka; K Tada; N Fueki; I Takahashi; A Igarashi; T Takabayashi; R Baumgartner
Journal:  J Pediatr       Date:  1987-01       Impact factor: 4.406

Review 3.  European experience with prenatal diagnosis of congenital disease: a survey of 6121 cases.

Authors:  H Galjaard
Journal:  Cytogenet Cell Genet       Date:  1976
  3 in total
  2 in total

Review 1.  Prenatal diagnosis of enzyme defects.

Authors:  B Winchester
Journal:  Arch Dis Child       Date:  1990-01       Impact factor: 3.791

2.  Prenatal diagnosis of non-ketotic hyperglycinaemia.

Authors:  J R Toone; D A Applegarth; H L Levy
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
  2 in total

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