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Volumn , Issue 289, 2003, Pages 73-77
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Heterochromia of the irides and a motility disorder of the oesophagus: a coincidence or a defect during embryogenesis?
a
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Author keywords
[No Author keywords available]
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Indexed keywords
ARTICLE;
CASE REPORT;
CONGENITAL MALFORMATION;
ESOPHAGITIS;
ESOPHAGUS FUNCTION DISORDER;
FEMALE;
HUMAN;
IRIS;
PRESCHOOL CHILD;
CHILD, PRESCHOOL;
ESOPHAGEAL MOTILITY DISORDERS;
ESOPHAGITIS;
FEMALE;
HUMANS;
IRIS;
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EID: 0642274806
PISSN: 00810746
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (1)
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References (0)
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