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Volumn 59, Issue 3, 2010, Pages 129-137
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Oral and craniofacial findings in a patient with methylmalonic aciduria and homocystinuria: review and a case report.
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Author keywords
[No Author keywords available]
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Indexed keywords
METHYLMALONIC ACID;
CASE REPORT;
CHILD;
CONGENITAL MALFORMATION;
CRANIOFACIAL MALFORMATION;
CYANOCOBALAMIN DEFICIENCY;
FACE;
FEMALE;
HOMOCYSTINURIA;
HUMAN;
INBORN ERROR OF METABOLISM;
MULTIPLE MALFORMATION SYNDROME;
PHENOTYPE;
REVIEW;
TOOTH MALFORMATION;
URINE;
ABNORMALITIES, MULTIPLE;
CHILD;
CRANIOFACIAL ABNORMALITIES;
FACE;
FEMALE;
HOMOCYSTINURIA;
HUMANS;
METABOLISM, INBORN ERRORS;
METHYLMALONIC ACID;
PHENOTYPE;
TOOTH ABNORMALITIES;
VITAMIN B 12 DEFICIENCY;
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EID: 77956633913
PISSN: 00264970
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
Times cited : (6)
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References (15)
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