Literature DB >> 4730942

Pre-symptomatic detection and genetic counselling in myotonic dystrophy.

P S Harper.   

Abstract

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Year:  1973        PMID： 4730942     DOI： 10.1111/j.1399-0004.1973.tb01134.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  6 in total

1.  Congenital myotonic dystrophy in Britain. II. Genetic basis.

Authors:  P S Harper
Journal:  Arch Dis Child       Date:  1975-07       Impact factor: 3.791

2.  Myotonic dystrophy--early detection and genetic counselling.

Authors:  T Schubert; F Jerusalem; A C Martenet; M Metaxas; M Meyer
Journal:  J Neurol       Date:  1980       Impact factor: 4.849

3.  Myotonic dystrophy- early detection and genetic counselling by T. Schubert et al.

Authors:  S Bundey
Journal:  J Neurol       Date:  1982       Impact factor: 4.849

4.  Cataract and myotonic dystrophy: the role of molecular diagnosis.

Authors:  W Reardon; J C MacMillan; J Myring; H G Harley; S A Rundle; L Beck; P S Harper; D J Shaw
Journal:  Br J Ophthalmol       Date:  1993-09       Impact factor: 4.638

5.  Hereditary cerebellar ataxia and genetic linkage with HLA.

Authors:  D Kumar; C E Blank; K Gelsthorpe
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

6.  Origin of a regressed myotonic dystrophy allele.

Authors:  M Giordano; M S De Angelis; R Mutani; P M Richiardi
Journal:  J Med Genet       Date:  1994-02       Impact factor: 6.318
  6 in total

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