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Volumn 107, Issue 1, 2002, Pages 5-11
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Camurati-Engelmann disease type II: Progressive diaphyseal dysplasia with striations of the bones
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Author keywords
Camurati Engelmann disease; Hyperostosis generalisata with striations of the bones; Progressive diaphyseal dysplasia; Transforming growth factor beta 1
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Indexed keywords
ALKALINE PHOSPHATASE;
DNA FRAGMENT;
TRANSFORMING GROWTH FACTOR BETA1;
ADOLESCENT;
ARTICLE;
CAMURATI ENGELMANN DISEASE TYPE II;
CASE REPORT;
CHILD;
CLINICAL FEATURE;
CRANIOFACIAL SYNOSTOSIS;
DIAGNOSTIC PROCEDURE;
DIAPHYSIS DYSPLASIA;
DISEASE CLASSIFICATION;
ERYTHROCYTE SEDIMENTATION RATE;
EXON;
FEMALE;
FLEXION CONTRACTURE;
GAIT DISORDER;
GENE MUTATION;
HIP DISEASE;
HUMAN;
HYPEROSTOSIS;
KNEE DISEASE;
LEG PAIN;
MARFAN SYNDROME;
METAPHYSIS;
MUSCLE WEAKNESS;
POLYMERASE CHAIN REACTION;
PRIORITY JOURNAL;
SEXUAL DEVELOPMENT;
SINGLE STRAND CONFORMATION POLYMORPHISM;
TRABECULAR BONE;
ACTIVIN RECEPTORS, TYPE I;
ADOLESCENT;
BONE AND BONES;
CAMURATI-ENGELMANN SYNDROME;
CHILD;
FEMALE;
HAND;
HUMANS;
LEG;
PELVIS;
RECEPTORS, TRANSFORMING GROWTH FACTOR BETA;
SKULL;
SPINE;
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EID: 0036135459
PISSN: 01487299
EISSN: None
Source Type: Journal
DOI: 10.1002/ajmg.10079 Document Type: Article |
Times cited : (26)
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References (9)
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