Journal of Medical Genetics


ISSN: 0022-2593        年代:1977
当前卷期:Volume 14  issue 2     [ 查看所有卷期 ]

年代:1977
 
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1. Occurrence of childhood cancers among sibs and estimation of familial risks.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  81-90

G JDraper,   M MHeaf,   L MKinnier Wilson,  

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2. Heterozygote detection in angiokeratoma corporis diffusum (Anderson-Fabry disease). Studies on plasma, leucocytes, and hair follicles.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  91-99

M WSpence,   A LGoldbloom,   J KBurgess,   DD'entremont,   B ARipley,   K LWeldon,  

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3. Rapid prenatal diagnosis of the Lesch-Nyhan syndrome.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  100-102

DHalley,   M JHeukels-Dully,  

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4. Genetic heterogeneity within the chondroitinsulphaturias.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  103-107

B SDanes,   B KRottell,   LEviatar,   JStolzenberg,  

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5. Problem of sex ratio in cases of type I syndactyly.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  108-113

C MWoolf,   D LCone,  

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6. Familial translocation with partial trisomy of 13 and 22: evidence that specific regions of chromosomes 13 and 22 are responsible for the phenotype of each trisomy.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  114-119

H JKim,   L YHsu,   L CGoldsmith,   LStrauss,   KHirschhorn,  

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7. Prenatal diagnosis and gonadal findings in X/XXX mosaicism.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  120-123

GKohn,   M MCohen,   YBeyth,   AOrnoy,  

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8. Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  124-127

JSimpson,   HZellweger,  

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9. Gonadal dysgenesis with Graves's disease.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  128-129

W HBrooks,   J CMeek,   R NSchimke,  

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10. Family in which Duchenne's muscular dystrophy and protan colour blindness are segregating.
  Journal of Medical Genetics,   Volume  14,   Issue  2,   1977,   Page  130-132

D NGreig,  

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