Journal of Medical Genetics


ISSN: 0022-2593        年代:1992
当前卷期:Volume 29  issue 5     [ 查看所有卷期 ]

年代:1992
 
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1. Cone and cone-rod dystrophies.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  289-290

A TMoore,  

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2. X linked progressive cone dystrophy with specific attention to carrier detection.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  291-294

J Avan Everdingen,   L NWent,   J EKeunen,   J AOosterhuis,  

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3. Late onset dominant cone dystrophy with early blue cone involvement.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  295-298

L NWent,   M Jvan Schooneveld,   J AOosterhuis,  

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4. Reverse chromosome painting: a method for the rapid analysis of aberrant chromosomes in clinical cytogenetics.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  299-307

N PCarter,   M AFerguson-Smith,   M TPerryman,   HTelenius,   A HPelmear,   M ALeversha,   M TGlancy,   S LWood,   KCook,   H MDyson,  

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5. Prenatal cystic fibrosis carrier testing: designing an information leaflet to meet the specific needs of the target population.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  308-312

M EMennie,   W AListon,   D JBrock,  

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6. Principles and practicalities of carrier screening: attitudes of recent parents.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  313-319

J MGreen,  

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7. Familial screening for genetic haemochromatosis by means of DNA markers.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  320-322

JYaouanq,   Ael Kahloun,   MChorney,   A MJouanolle,   VMauvieux,   MPerichon,   MBlayau,   PPontarotti,   J YLe Gall,   VDavid,  

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8. Ectodermal dysplasia with blindness in sibs on the island of Rodrigues.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  323-325

C EWallis,   PBeighton,  

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9. Oculoauriculovertebral spectrum and cerebral anomalies.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  326-331

C TSchrander-Stumpel,   C Ede Die-Smulders,   R CHennekam,   J PFryns,   P XBouckaert,   O FBrouwer,   J Jda Costa,   E JLommen,   P DMaaswinkel-Mooy,  

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10. Weaver syndrome.
  Journal of Medical Genetics,   Volume  29,   Issue  5,   1992,   Page  332-337

T RCole,   N RDennis,   H EHughes,  

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