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- [1] A de novo 3p13 deletion induced by a complex chromosomal rearrangement combined with a pericentric inversion of chromosome 3, inv(3)(p13q12), and a translocation between chromosome 3 and 8, t(3;8)(q13.1;q24.2), in a child with developmental delay (vol 39, pg 121, 2017) GENES & GENOMICS, 2017, 39 (02) : 243 - 243
- [2] CASE OF CHROMOSOME-3 DUPLICATION-Q DELETION-P SYNDROME BORN TO THE MOTHER WITH A PERICENTRIC-INVERSION, INV(3)(P25Q21) JAPANESE JOURNAL OF HUMAN GENETICS, 1979, 24 (01): : 9 - 12
- [3] CASE OF CHROMOSOME-3 DUPLICATION-Q DELETION-P SYNDROME BORN TO THE MOTHER WITH A PERICENTRIC-INVERSION, INV(3) (P25Q21) JAPANESE JOURNAL OF HUMAN GENETICS, 1979, 24 (03): : 161 - 162
- [7] De novo complex chromosomal rearrangement of 46, XY, t (3; 16; 8) (p26; q13; q21.2) in a non-obstructive azoospermic male Journal of Applied Genetics, 2007, 48 : 93 - 94
- [9] A novel t(3;8)(p13;q21.1) translocation in a case of lipoblastoma Pediatric Surgery International, 2012, 28 : 737 - 740
- [10] Identification of a yeast artificial chromosome spanning the 8q12 translocation breakpoint in pleomorphic adenomas with t(3;8)(p21;q12) GENES CHROMOSOMES & CANCER, 1996, 17 (03): : 166 - 171