Journal of Medical Genetics


ISSN: 0022-2593        年代:1989
当前卷期:Volume 26  issue 6     [ 查看所有卷期 ]

年代:1989
 
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1. Different options for prenatal testing for Huntington's disease using DNA probes.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  353-357

MFahy,   CRobbins,   MBloch,   R WTurnell,   M RHayden,  

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2. Clinical variability of osteogenesis imperfecta linked to COL1A2 and associated with a structural defect in the type I collagen molecule.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  358-362

ASuperti-Furga,   FPistone,   CRomano,   BSteinmann,  

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3. Prenatal diagnosis of beta thalassaemia based on restriction endonuclease analysis of amplified fetal DNA.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  363-367

MPirastu,   M SRistaldi,   ACao,  

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4. Ultrasound in the perinatal necropsy.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  368-372

M EFurness,   R CWeckert,   S AParker,   SKnowles,  

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5. X linked mental retardation: a family with a separate syndrome?
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  373-378

E MThompson,   AGordon,   MBaraitser,  

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6. Chromosome studies of males in an institution for the mentally handicapped.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  379-381

C JEnglish,   E VDavison,   M SBhate,   LBarrett,  

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7. Hypertrichosis cubiti (hairy elbows) and short stature: a recognisable association.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  382-385

K DMacDermot,   M APatton,   M JWilliams,   R MWinter,  

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8. Dominantly inherited cleft lip and palate in two families.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  386-389

KTemple,   MCalvert,   DPlint,   EThompson,   MPembrey,  

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9. Population frequencies of three DNA alleles linked to the Duchenne muscular dystrophy gene.
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  390-392

S SPapiha,   D FRoberts,   AClarke,   JBurn,   DGardner-Medwin,   S SBhattacharya,  

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10. Cranioectodermal dysplasia (Sensenbrenner's syndrome).
  Journal of Medical Genetics,   Volume  26,   Issue  6,   1989,   Page  393-396

I DYoung,  

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