Literature DB >> 2890881

Prenatal diagnosis of congenital adrenal hyperplasia.

T Strachan, P J Sinnott, I Smeaton, P A Dyer, R Harris.   

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Year:  1987        PMID： 2890881     DOI： 10.1016/s0140-6736(87)91880-0

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


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  11 in total

Review 1.  An overview of molecular diagnosis of steroid 21-hydroxylase deficiency.

Authors:  C E Keegan; A A Killeen
Journal:  J Mol Diagn       Date:  2001-05       Impact factor: 5.568

2.  Colchicine myoneuropathy and renal dysfunction.

Authors:  S A Older; D S Finbloom; G H Pezeshkpour
Journal:  Ann Rheum Dis       Date:  1992-12       Impact factor: 19.103

3.  In vitro gene amplification for prenatal diagnosis of congenital adrenal hyperplasia.

Authors:  G Rumsby; J W Honour
Journal:  J Med Genet       Date:  1990-11       Impact factor: 6.318

4.  Molecular genetics in the National Health Service in Britain.

Authors:  R Harris; R Elles; D Craufurd; A Dodge; A Ivinson; K Hodgkinson; R Mountford; M Schwartz; T Strachan; A Read
Journal:  J Med Genet       Date:  1989-04       Impact factor: 6.318

5.  21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

Authors:  P J Sinnott; P A Dyer; D A Price; R Harris; T Strachan
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

6.  Prenatal diagnosis and management of congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.

Authors:  E Passarge
Journal:  Indian J Pediatr       Date:  1988 Jul-Aug       Impact factor: 1.967

7.  Prenatal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency by allele-specific hybridization and Southern blot.

Authors:  P W Speiser; P C White; J Dupont; D Zhu; A B Mercado; M I New
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

8.  Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis.

Authors:  M Lako; S Ramsden; R D Campbell; T Strachan
Journal:  J Med Genet       Date:  1999-02       Impact factor: 6.318

Review 9.  Molecular pathology of 21-hydroxylase deficiency.

Authors:  T Strachan
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

10.  Family studies of the steroid 21-hydroxylase and complement C4 genes define 11 haplotypes in classical congenital adrenal hyperplasia in The Netherlands.

Authors:  P F Koppens; T Hoogenboezem; D J Halley; C A Barendse; A J Oostenbrink; H J Degenhart
Journal:  Eur J Pediatr       Date:  1992-12       Impact factor: 3.183
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