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Volumn 306, Issue 5696, 2004, Pages
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The critical region in trisomy 21
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Author keywords
[No Author keywords available]
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Indexed keywords
SCIENCE AND TECHNOLOGY;
CHROMOSOME DELETION;
CHROMOSOME DUPLICATION;
CRANIOFACIAL MALFORMATION;
DOWN SYNDROME;
DSCR GENE;
GENE;
GENETIC DISORDER;
GENETIC ENGINEERING;
GENETIC RECOMBINATION;
HEMOPHILIA;
HUMAN;
MOUSE;
NONHUMAN;
PHENOTYPE;
PRIORITY JOURNAL;
REVIEW;
TRISOMY 21;
ZELLWEGER SYNDROME;
ANIMAL;
CHROMOSOME;
CHROMOSOME 21;
CONGENITAL MALFORMATION;
CROSS BREEDING;
DISEASE MODEL;
FEMALE;
GENE DUPLICATION;
GENETICS;
MALE;
NOTE;
PATHOLOGY;
SKULL;
TRISOMY;
ANIMALS;
CHROMOSOME DELETION;
CHROMOSOMES, HUMAN, PAIR 21;
CHROMOSOMES, MAMMALIAN;
CRANIOFACIAL ABNORMALITIES;
CROSSES, GENETIC;
DISEASE MODELS, ANIMAL;
DOWN SYNDROME;
FEMALE;
GENE DUPLICATION;
HUMANS;
MALE;
MICE;
RECOMBINATION, GENETIC;
SKULL;
TRISOMY;
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EID: 7444229867
PISSN: 00368075
EISSN: None
Source Type: Journal
DOI: 10.1126/science.1105226 Document Type: Review |
Times cited : (29)
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References (10)
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