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- [25] IDENTIFICATION OF MICRODELETIONS SPANNING THE DIAMOND-BLACKFAN ANEMIA (DBA) LOCUS ON 19Q13 AND EVIDENCE FOR GENETIC HETEROGENEITY Pediatric Research, 1999, 45 : 941 - 941
- [26] ASSIGNMENT OF THE HUMAN UROKINASE RECEPTOR GENE (PLAUR) TO 19Q13 CYTOGENETICS AND CELL GENETICS, 1992, 60 (3-4): : 197 - 199
- [28] LINKAGE AND ASSOCIATION OF MARKERS AT 7Q21.3-]Q22.1 WITH NON-INSULIN-DEPENDENT DIABETES-MELLITUS (NIDDM) IN PIMA-INDIANS CYTOGENETICS AND CELL GENETICS, 1995, 71 (01): : 30 - 30
- [29] Deletion of 19q13 reveals clinical overlap with Dubowitz syndrome Journal of Human Genetics, 2015, 60 : 781 - 785