共 47 条
- [5] Search for genes involved in Joubert syndrome:: Evidence that one or more major loci are yet to be identified and exclusion of candidate genes EN1, EN2, FGF8, and BARHL1 [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 107 (03): : 190 - 196
- [6] JOUBERT SYNDROME - EPISODIC HYPERPNEA, ABNORMAL EYE-MOVEMENTS, RETARDATION AND ATAXIA, ASSOCIATED WITH DYSPLASIA OF CEREBELLAR VERMIS [J]. NEUROPADIATRIE, 1977, 8 (01): : 57 - 66
- [7] A NEW SYNDROME WITH FEATURES OF THE SMITH-LEMLI-OPITZ AND MECKEL-GRUBER SYNDROMES IN A SIBSHIP WITH CEREBELLAR DEFECTS [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 26 (02): : 321 - 336
- [10] Dahlstrom JE, 2000, PATHOLOGY, V32, P283