|
Volumn 318, Issue 7190, 1999, Pages 1019-1020
|
Tuberous sclerosis
|
Author keywords
[No Author keywords available]
|
Indexed keywords
CENTRAL NERVOUS SYSTEM DISEASE;
CLINICAL FEATURE;
DIAGNOSTIC IMAGING;
EDITORIAL;
EPILEPSY;
GENETIC COUNSELING;
GENETICS;
HUMAN;
KIDNEY DISEASE;
LEARNING DISORDER;
MOLECULAR GENETICS;
PATHOPHYSIOLOGY;
PRIORITY JOURNAL;
SKIN DISEASE;
TUBEROUS SCLEROSIS;
TUMOR SUPPRESSOR GENE;
UNITED KINGDOM;
|
EID: 0033577488
PISSN: 09598146
EISSN: None
Source Type: Journal
DOI: 10.1136/bmj.318.7190.1019 Document Type: Editorial |
Times cited : (32)
|
References (13)
|