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Volumn 139, Issue 6, 2001, Pages 892-895
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Graves' disease in patients with 22q11.2 deletion
a,b,c,d a,b,c,d a,b,c,d a,b,c,d a,b,c,d a,b,c,d a,b,c,d a,b,c,d a,b,c,d a,b,c,d |
Author keywords
[No Author keywords available]
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Indexed keywords
THYROID HORMONE;
THYROTROPIN;
ADOLESCENT;
ADULT;
ARTICLE;
AUTOIMMUNE DISEASE;
CASE REPORT;
CHILD;
CHROMOSOME 22Q;
CHROMOSOME DELETION;
CLINICAL FEATURE;
DIGEORGE SYNDROME;
FEMALE;
FLUORESCENCE IN SITU HYBRIDIZATION;
GRAVES DISEASE;
HUMAN;
HYPERTHYROIDISM;
PHENOTYPE;
PRIORITY JOURNAL;
SEIZURE;
THYROID HORMONE BLOOD LEVEL;
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EID: 0035659620
PISSN: 00223476
EISSN: None
Source Type: Journal
DOI: 10.1067/mpd.2001.119448 Document Type: Article |
Times cited : (53)
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References (12)
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