| Hereditary characteristics of enzyme deficiency and dermatoglyphics in congenital color blindness. | |
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MedLine Citation:
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PMID: 3263528 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The hereditary characteristics of enzyme deficiency and dermatoglyphics in congenital color blindness (CCB) were studied. We propose that there is a linkage between the two loci on the X-chromosome determining CCB and glucose-6-phosphate dehydrogenase (G6PD), based on our study of a high incidence of G6PD deficiency in 156 male cases with CCB. The CCB gene is closely linked with that of G6PD deficiency from our pedigree investigations. The rise in the frequency of eight or more whorls, the low value of atd angle and the presenting rate of real palmar patterns of the thenar, hypothenar and I, areas presented the hereditary traits of congenital color blindness. |
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Authors:
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L Z Wu; L H Zeng; Q Y Ma; Y J Xie; Y Z Chen; D Z Wu |
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Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't |
Journal Detail:
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Title: Japanese journal of ophthalmology Volume: 32 ISSN: 0021-5155 ISO Abbreviation: Jpn. J. Ophthalmol. Publication Date: 1988 |
Date Detail:
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Created Date: 1988-12-08 Completed Date: 1988-12-08 Revised Date: 2006-11-15 |
Medline Journal Info:
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Nlm Unique ID: 0044652 Medline TA: Jpn J Ophthalmol Country: JAPAN |
Other Details:
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Languages: eng Pagination: 236-45 Citation Subset: IM |
Affiliation:
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Eye Research Institute, Zhongshan Ophthalmic Center, Sun Yat-Sen University of Medical Sciences, Guangzhou, China. |
Export Citation:
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| MeSH Terms | |
Descriptor/Qualifier:
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Color Vision Defects
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congenital,
genetics* Dermatoglyphics* Female Glucosephosphate Dehydrogenase Deficiency / genetics* Humans Linkage (Genetics) Male Pedigree Sex Characteristics |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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