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机译:埃及家庭的神经发育障碍,双胞胎alkbh8变体
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Natl Res Ctr Dept Clin Genet Human Genet &
Genome Res Div Cairo Egypt;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Baylor Coll Med Human Genome Sequencing Ctr Houston TX USA;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Baylor Coll Med Dept Radiol Houston TX 77030 USA;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
Natl Res Ctr Dept Clin Genet Human Genet &
Genome Res Div Cairo Egypt;
Baylor Coll Med Dept Mol &
Human Genet One Baylor Plaza Room 604B Houston TX 77030 USA;
ALKBH8; intellectual disability; neurodevelopmental delay; tRNA modification;
机译:在兄弟姐妹中的rbl2中的双射击函数变体具有神经发育障碍
机译:扩大表型:神经发育障碍,线粒体,具有异常运动和乳酸性能,由于WARS2双腿变体因WATS2双晶型变体而有或没有癫痫发作(NEMMLAS),编码线粒体色氨酸-TRNA合酶
机译:扩大表型:神经发育障碍,线粒体,具有异常运动和乳酸性能,由于WARS2双腿变体因WATS2双晶型变体而有或没有癫痫发作(NEMMLAS),编码线粒体色氨酸-TRNA合酶
机译:超准确的复杂性疾病预测:神经发育障碍的案例研究
机译:精神分裂症和双相情感障碍的突触前和神经发育候选基因变异的传播分析。
机译:KCNK18与智力残疾相关的双胞胎变体和神经发育障碍改变了TRESK频道活动
机译:双胞胎丧失函数变体InRBL2IN兄弟姐妹具有神经发育障碍
机译:改变胎盘色氨酸代谢:神经发育障碍胎儿编程的关键分子途径。