Journal of Medical Genetics


ISSN: 0022-2593        年代:1986
当前卷期:Volume 23  issue 5     [ 查看所有卷期 ]

年代:1986
 
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1. Medical genetics in China: a western view.
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  385-388

P SHarper,   RHarris,  

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2. Williams syndrome.
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  389-395

JBurn,  

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3. The frequency of the fragile X chromosome among schoolchildren in Coventry.
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  396-399

T PWebb,   SBundey,   AThake,   JTodd,  

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4. Twelve families with fragile X(q27).
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  400-406

TWebb,   AThake,   JTodd,  

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5. Replication status of fragile X(q27.3) in 13 female heterozygotes.
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  407-410

ETuckerman,   TWebb,   AThake,  

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6. Mutations linked to the pro alpha 2(I) collagen gene are responsible for several cases of osteogenesis imperfecta type I.
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  411-416

GWallis,   PBeighton,   CBoyd,   C GMathew,  

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7. A model system for the analysis of gene exclusion: cystic fibrosis and chromosome 19.
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  417-420

BWainwright,   MFarrall,   EWatson,   RWilliamson,  

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8. A new strategy for mapping the human genome.
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  421-424

D JShaw,  

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9. Pseudoachondroplasia: clinical diagnosis at different ages and comparison of autosomal dominant and recessive types. A review of 32 patients (26 kindreds).
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  425-434

RWynne-Davies,   C MHall,   I DYoung,  

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10. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).
  Journal of Medical Genetics,   Volume  23,   Issue  5,   1986,   Page  435-445

JBrusnický,   K Mvan Heerden,   Gde Jong,   A SCronjé,   A ERetief,  

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