...
机译:De Novo突变在Med13中,介质复合物的组分,与新的神经发育障碍有关
Radboud Univ Nijmegen Human Genet Dept Med Ctr POB 9101 NL-6500 HB Nijmegen Netherlands;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL 35806 USA;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL 35806 USA;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL 35806 USA;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL 35806 USA;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL 35806 USA;
Univ Alabama Birmingham Birmingham AL USA;
Leiden Univ Dept Clin Genet Med Ctr Leiden Netherlands;
Leiden Univ Dept Clin Genet Med Ctr Leiden Netherlands;
Univ Utrecht Univ Med Ctr Utrecht Dept Genet Leiden Netherlands;
Univ Utrecht Univ Med Ctr Utrecht Dept Genet Leiden Netherlands;
Maine Med Ctr Dept Pediat Div Genet Portland ME 04102 USA;
Great Ormond St Hosp Sick Children London England;
GeneDx 207 Perry Pkwy Gaithersburg MD 20877 USA;
GeneDx 207 Perry Pkwy Gaithersburg MD 20877 USA;
GeneDx 207 Perry Pkwy Gaithersburg MD 20877 USA;
Baylor Coll Med Dept Mol &
Human Genet Houston TX 77030 USA;
Baylor Coll Med Dept Mol &
Human Genet Houston TX 77030 USA;
Univ Glasgow Paediat Neurosci Res Grp Glasgow G51 4TF Lanark Scotland;
Univ Glasgow Paediat Neurosci Res Grp Glasgow G51 4TF Lanark Scotland;
Univ Oxford Wellcome Ctr Human Genet Oxford England;
Ann &
Robert H Lurie Childrens Hosp Chicago Chicago IL 60611 USA;
Cincinnati Childrens Hosp Med Ctr Div Human Genet Cincinnati OH 45229 USA;
Cincinnati Childrens Hosp Med Ctr Div Human Genet Cincinnati OH 45229 USA;
Childrens Hosp Philadelphia Div Neurol Philadelphia PA 19104 USA;
Childrens Hosp Philadelphia Div Neurol Philadelphia PA 19104 USA;
Radboud Univ Nijmegen Human Genet Dept Med Ctr POB 9101 NL-6500 HB Nijmegen Netherlands;
Radboud Univ Nijmegen Human Genet Dept Med Ctr POB 9101 NL-6500 HB Nijmegen Netherlands;
Max Planck Inst Psycholinguist Language &
Genet Dept Nijmegen Netherlands;
Radboud Univ Nijmegen Human Genet Dept Med Ctr POB 9101 NL-6500 HB Nijmegen Netherlands;
HudsonAlpha Inst Biotechnol 601 Genome Way Huntsville AL 35806 USA;
机译:De Novo突变在Med13中,介质复合物的组分,与新的神经发育障碍有关
机译:中国患者中的三个额外的Novo CTCF突变有助于定义新兴的神经发育障碍
机译:de novo畸打突变的空间聚类鉴定了候选神经发育障碍相关基因
机译:超精确的复杂疾病预测:神经发育疾病的案例研究
机译:神经发育障碍中的Novo畸形突变
机译:MED13(介体复合物的组成部分)中的从头突变与新型神经发育障碍相关
机译:Med13中的Novo突变是介质复合物的组分,与新的神经发育障碍有关
机译:质粒pKm101介导的复杂移码突变:由4-氨基联苯诱导的沙门氏菌突变谱引起的突变机制