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Volumn 27, Issue 5, 1997, Pages 454-
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Heterogeneity in Schwartz-Jampel chondrodystrophic myotonia [1]
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Author keywords
[No Author keywords available]
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Indexed keywords
BONE DYSPLASIA;
CHROMOSOME 1Q;
CLINICAL FEATURE;
DISEASE CLASSIFICATION;
DISEASE COURSE;
GENE LOCUS;
GENETIC HETEROGENEITY;
GENETIC LINKAGE;
HUMAN;
LETTER;
MAJOR CLINICAL STUDY;
MYOTONIA;
ONSET AGE;
PRIORITY JOURNAL;
RECESSIVE INHERITANCE;
SCHWARTZ JAMPEL SYNDROME;
SHORT STATURE;
HUMANS;
OSTEOCHONDRODYSPLASIAS;
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EID: 0030923243
PISSN: 03010449
EISSN: None
Source Type: Journal
DOI: 10.1007/s002470050168 Document Type: Letter |
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Times cited : (2)
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References (1)
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