| 11. |
Cataracts as a marker of genetic heterogeneity in chondrodysplasia punctata |
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Clinical Genetics,
Volume 19,
Issue 1,
1981,
Page 64-66
Rudolf Happle,
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摘要:
Cataracts are suggested as a diagnostic marker to differentiate between the three types of chondrodysplasia punctata so far known. Both the rhizomelic and the X‐linked dominant types are associated with cataracts in about two‐thirds of the cases. In the rhizomelic type, the opacities tend to be bilateral and symmetrical. In the X‐linked dominant type they are usually asymmetrical and often unilateral. In contrast, the consistent lack of cataracts is characteristic of the autosomal dominant type of chondrodysplasia pun
ISSN:0009-9163
DOI:10.1111/j.1399-0004.1981.tb00669.x
出版商:Blackwell Publishing Ltd
年代:1981
数据来源: WILEY
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| 12. |
Apparent influence of marker genotypes on variation in serum cholesterol in monozygotic twins |
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Clinical Genetics,
Volume 19,
Issue 1,
1981,
Page 67-70
P. Magnus,
K. Berg,
A.‐L. Børresen,
W. E. Nance,
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摘要:
Ninety‐seven monozygotic (MZ) twin pairs were grouped by marker system genotypes, and mean intrapair differences in serum total cholesterol level were compared between groups. Significant differences were found when the MNSs and the Kidd blood group systems were considered. The results appear to suggest a restrictive effect of certain normal marker genes on environmentally caused variation in serum cholesterol leve
ISSN:0009-9163
DOI:10.1111/j.1399-0004.1981.tb00670.x
出版商:Blackwell Publishing Ltd
年代:1981
数据来源: WILEY
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| 13. |
Roberts's syndrome |
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Clinical Genetics,
Volume 19,
Issue 1,
1981,
Page 71-74
Elaine Louie,
James German,
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ISSN:0009-9163
DOI:10.1111/j.1399-0004.1981.tb00671.x
出版商:Blackwell Publishing Ltd
年代:1981
数据来源: WILEY
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| 14. |
Incidence of major chromosomal abnormalities |
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Clinical Genetics,
Volume 19,
Issue 1,
1981,
Page 75-76
K. Méhes,
Katzalin. Bajnóczky,
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ISSN:0009-9163
DOI:10.1111/j.1399-0004.1981.tb00672.x
出版商:Blackwell Publishing Ltd
年代:1981
数据来源: WILEY
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| 15. |
Familial sex chromosome mosaicism (yes) and interchromosomal effects (no) |
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Clinical Genetics,
Volume 19,
Issue 1,
1981,
Page 77-78
Frederick Hecht,
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ISSN:0009-9163
DOI:10.1111/j.1399-0004.1981.tb00673.x
出版商:Blackwell Publishing Ltd
年代:1981
数据来源: WILEY
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| 16. |
International Conference on Dermatoglyphics |
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Clinical Genetics,
Volume 19,
Issue 1,
1981,
Page 79-80
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PDF (113KB)
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ISSN:0009-9163
DOI:10.1111/j.1399-0004.1981.tb00674.x
出版商:Blackwell Publishing Ltd
年代:1981
数据来源: WILEY
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Volume 19 issue 1