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Volumn 50, Issue 4, 1992, Pages 690-699
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Maternal uniparental isodisomy of chromosome 14: Association with autosomal recessive rod monochromacy
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
ADULT;
ARTICLE;
AUTOSOMAL RECESSIVE DISORDER;
CASE REPORT;
CHROMOSOME 14;
CHROMOSOME MARKER;
CLINICAL FEATURE;
COLOR BLINDNESS;
CONTROLLED STUDY;
CYTOGENETICS;
DENSITOMETRY;
FEMALE;
HUMAN;
HUMAN CELL;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
RESTRICTION FRAGMENT LENGTH POLYMORPHISM;
ROBERTSONIAN CHROMOSOME TRANSLOCATION;
SOUTHERN BLOTTING;
CASE REPORT;
CHROMOSOME MAPPING;
CHROMOSOMES, HUMAN, PAIR 14;
FEMALE;
HETEROZYGOTE DETECTION;
HOMOZYGOTE;
HUMAN;
INFANT, NEWBORN;
KARYOTYPING;
PHOTORECEPTORS;
POLYMORPHISM (GENETICS);
POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;
RETINAL DISEASES;
SUPPORT, NON-U.S. GOV'T;
TRANSLOCATION (GENETICS);
ROBERTSONIA;
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EID: 0026574487
PISSN: 00029297
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (113)
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References (0)
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