机译:8p染色体部分三体性与自闭症相关的一例
Department of Child Psychiatry University of Athens “Agia Sophia” Children’s Hospital 115 27 Athens Greece;
Department of Child Psychiatry University of Athens “Agia Sophia” Children’s Hospital 115 27 Athens Greece;
Department of Genetics Institute of Child Health “Agia Sophia” Children’s Hospital 115 27 Athens Greece;
Department of Child Psychiatry University of Athens “Agia Sophia” Children’s Hospital 115 27 Athens Greece;
Department of Child Psychiatry University of Athens “Agia Sophia” Children’s Hospital 115 27 Athens Greece;
Department of Genetics Institute of Child Health “Agia Sophia” Children’s Hospital 115 27 Athens Greece;
Department of Child Psychiatry University of Athens “Agia Sophia” Children’s Hospital 115 27 Athens Greece;
Autism; Genetics; Chromosome 8; Partial trisomy 8p;
机译:部分单粒子8P(8P23.2→Pter)和部分三兆癣15Q(15Q21.2→qter)的诊断和偶然染色体血液迁移的偶然检测与颈部半透明和异常母体血清筛选结果相关
机译:西部综合征,伴有新的染色体异常;家族性不平衡易位导致的部分三体性8P和部分性9P
机译:部分单体性13q(13q21.32 ---> qter)和部分三体性8p(8p1 ---> pter)表现为无脑并增加了颈部半透明性:阵列比较基因组杂交表征。
机译:Mayo诊所的三元和性染色体非细胞非染色体的无细胞DNA产前筛网管道
机译:染色体8p等位基因状态在前列腺癌进展中的意义
机译:一个家庭中有两个相互易位的部分三体性8p和部分单性21q(8; 21)(p21.1; q22.3)。
机译:部分单体13q(13q21.32→qter)和部分三体性8p(8p12→pter)呈现无脑畸形和增加的颈部半透明:阵列比较基因组杂交表征