Journal of Medical Genetics


ISSN: 0022-2593        年代:1989
当前卷期:Volume 26  issue 10     [ 查看所有卷期 ]

年代:1989
 
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1. The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  609-613

G AHitman,   LGarde,   WDaoud,   G JSnodgrass,  

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2. The molecular basis of beta thalassaemia in Bulgaria.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  614-618

LKalaydjieva,   AEigel,   JHorst,  

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3. A summary of 7q interstitial deletions and exclusion mapping of the gene for beta-glucuronidase.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  619-625

KFagan,   AGill,   RHenry,   IWilkinson,   BCarey,  

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4. Alternate centromere inactivation in a pseudodicentric (15;20)(pter;pter) associated with a progressive neurological disorder.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  626-630

HRivera,   OZuffardi,   PMaraschio,   ACaiulo,   CAnichini,   RScarinci,   RVivarelli,  

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5. Transient nephrotic syndrome after anaesthesia resulting from a familial cryofibrinogen precipitating at 35 degrees C.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  631-636

YLolin,   P ARazis,   PO'Gorman,   MHjelm,   A SWierzbicki,  

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6. Emery-Dreifuss syndrome.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  637-641

A EEmery,  

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7. Familial mental retardation associated with balanced chromosome rearrangement rcp t(8;11)(q24.3;p15.1).
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  642-644

HSato,   KTakaya,   SNihira,   HFujita,  

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8. A new interstitial deletion of 4q (q21.1::q22.1).
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  644-647

KFagan,   AGill,  

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9. Cat eye syndrome associated with aganglionosis of the small and large intestine.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  647-648

JWard,   I ASierra,   ED'Croz,  

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10. A single maxillary incisor as a manifestation of an ectodermal dysplasia.
  Journal of Medical Genetics,   Volume  26,   Issue  10,   1989,   Page  648-651

IBuntinx,   MBaraitser,  

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