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Volumn 111, Issue 3, 2002, Pages 297-298
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Favourable mutation test outcomes for individuals at risk for Huntington disease change the perspectives of first-degree relatives
a
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA;
ADULT;
AUTOSOMAL DOMINANT DISORDER;
CHILD;
DISEASE PREDISPOSITION;
DNA DETERMINATION;
FAMILIAL CANCER;
FAMILY;
GENETIC COUNSELING;
GENETIC SCREENING;
GENOTYPE;
HETEROZYGOTE DETECTION;
HIGH RISK POPULATION;
HOMOZYGOSITY;
HUMAN;
HUNTINGTON CHOREA;
MUTATIONAL ANALYSIS;
PARENT;
PREGNANCY;
PRENATAL DIAGNOSIS;
PRIORITY JOURNAL;
PROBABILITY;
PROGENY;
RELATIVE;
RISK ASSESSMENT;
SHORT SURVEY;
SIBLING;
SPONTANEOUS ABORTION;
DNA MUTATIONAL ANALYSIS;
FEMALE;
GENETIC COUNSELING;
GENOTYPE;
HETEROZYGOTE DETECTION;
HUMANS;
HUNTINGTON DISEASE;
MALE;
NERVE TISSUE PROTEINS;
NUCLEAR PROTEINS;
PEDIGREE;
PREGNANCY;
PRENATAL DIAGNOSIS;
PROBABILITY;
RISK;
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EID: 0036765886
PISSN: 03406717
EISSN: None
Source Type: Journal
DOI: 10.1007/s00439-002-0764-9 Document Type: Short Survey |
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Times cited : (6)
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References (6)
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