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Volumn 18, Issue 6, 1982, Pages 629-644
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Lowe's syndrome
a a a a |
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Author keywords
[No Author keywords available]
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Indexed keywords
AMINO ACID URINE LEVEL;
CASE REPORT;
CATARACT;
CENTRAL NERVOUS SYSTEM;
CONGENITAL CATARACT;
CONGENITAL DISORDER;
CORNEA KELOID;
CORNEA OPACITY;
DIAGNOSIS;
ETIOLOGY;
GLAUCOMA;
HEREDITY;
HUMAN;
KIDNEY;
KIDNEY DISEASE;
LOWE SYNDROME;
MENTAL DEFICIENCY;
MENTAL RETARDATION MALFORMATION SYNDROME;
MIOSIS;
VISUAL SYSTEM;
CASE REPORT;
CHILD;
CHILD, PRESCHOOL;
CORNEA;
CORNEAL DISEASES;
FEMALE;
GENES, RECESSIVE;
HUMAN;
INFANT, NEWBORN;
KELOID;
LENS, CRYSTALLINE;
MALE;
OCULOCEREBRORENAL SYNDROME;
PEDIGREE;
RENAL TUBULAR TRANSPORT, INBORN ERRORS;
X CHROMOSOME;
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EID: 0020460944
PISSN: 05476844
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
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Times cited : (7)
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References (0)
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