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Volumn 50, Issue 2, 1996, Pages 112-
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Osteopenia, abnormal dentition, hydrops fetalis and communicating hydrocephalus: unusual early clinical signs in Coffin-Lowry syndrome.
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NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
CASE REPORT;
CLASSIFICATION;
CONGENITAL MALFORMATION;
FACE;
FETUS HYDROPS;
FINGER;
GENETICS;
HUMAN;
HYDROCEPHALUS;
MALE;
METABOLIC BONE DISEASE;
MULTIPLE MALFORMATION SYNDROME;
NOTE;
PRESCHOOL CHILD;
SYNDROME;
TOOTH MALFORMATION;
ABNORMALITIES, MULTIPLE;
BONE DISEASES, METABOLIC;
CHILD, PRESCHOOL;
FACE;
FINGERS;
HUMANS;
HYDROCEPHALUS;
HYDROPS FETALIS;
MALE;
SYNDROME;
TOOTH ABNORMALITIES;
MLCS;
MLOWN;
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EID: 0030202814
PISSN: 00099163
EISSN: None
Source Type: Journal
DOI: 10.1111/j.1399-0004.1996.tb02362.x Document Type: Note |
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Times cited : (6)
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References (0)
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