Literature DB >> 6631608

Outlook for a clinically normal child in a sibship with congenital myotonic dystrophy.

T O'Brien, R G Newcombe, P S Harper.   

Abstract

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Year:  1983        PMID： 6631608     DOI： 10.1016/s0022-3476(83)80480-6

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  4 in total

1.  Specific molecular prenatal diagnosis for the CTG mutation in myotonic dystrophy.

Authors:  J Myring; A L Meredith; H G Harley; G Kohn; G Norbury; P S Harper; D J Shaw
Journal:  J Med Genet       Date:  1992-11       Impact factor: 6.318

2.  Age at onset and life table risks in genetic counselling for Huntington's disease.

Authors:  P S Harper; R G Newcombe
Journal:  J Med Genet       Date:  1992-04       Impact factor: 6.318

3.  Genetic risks for children of women with myotonic dystrophy.

Authors:  M C Koch; T Grimm; H G Harley; P S Harper
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

4.  Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.

Authors:  K V Walsh; H G Harley; J D Brook; S A Rundle; M Sarfarazi; P S Harper; D J Shaw
Journal:  Hum Genet       Date:  1990-08       Impact factor: 4.132
  4 in total

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