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Volumn 4, Issue 2, 2007, Pages 97-105
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Why females are mosaics, x-chromosome inactivation, and sex differences in disease
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Author keywords
[No Author keywords available]
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Indexed keywords
DNA METHYLTRANSFERASE 3B;
EPHRIN B1;
TESTIS DETERMINING FACTOR;
ARTICLE;
AUTOIMMUNE DISEASE;
CHROMATIN ASSEMBLY AND DISASSEMBLY;
CHROMOSOME DELETION;
CHROMOSOME TRANSLOCATION;
DISEASE SEVERITY;
FABRY DISEASE;
GENE DELETION;
GENE EXPRESSION;
GENE EXPRESSION REGULATION;
GENE MUTATION;
GENETIC TRANSCRIPTION;
GENETIC VARIABILITY;
HETEROZYGOTE;
HUMAN;
HUNTER SYNDROME;
LESCH NYHAN SYNDROME;
MOLECULAR EVOLUTION;
MORTALITY;
NONHUMAN;
PATHOGENESIS;
PHENOTYPE;
PRIORITY JOURNAL;
SEX CHROMOSOME MOSAICISM;
SEX DIFFERENCE;
SEX DIFFERENTIATION;
SRY GENE;
TESTIS DEVELOPMENT;
X CHROMOSOME;
X CHROMOSOME INACTIVATION;
X CHROMOSOME LINKED DISORDER;
Y CHROMOSOME;
CHROMOSOMES, HUMAN, X;
FEMALE;
GENETIC DISEASES, X-LINKED;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
LIFE EXPECTANCY;
MALE;
MOSAICISM;
SEX CHARACTERISTICS;
SEX FACTORS;
X CHROMOSOME INACTIVATION;
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EID: 34547842802
PISSN: 15508579
EISSN: None
Source Type: Journal
DOI: 10.1016/S1550-8579(07)80024-6 Document Type: Article |
Times cited : (97)
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References (10)
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