机译:增强的MAPK1功能导致Rasopathy临床光谱内的神经发育障碍
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Univ Roma Tor Vergata Dept Chem Sci &
Technol I-00133 Rome Italy;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Ist Super Sanita Core Facil Microscopy Area I-00161 Rome Italy;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Ist Super Sanita Dept Oncol &
Mol Med I-00161 Rome Italy;
Vrije Univ Dept Clin Genet Amsterdam UMC NL-1117 Amsterdam Netherlands;
Univ Med Ctr Utrecht Dept Genet NL-3584 CX Utrecht Netherlands;
San Martino Hosp Med Genet Unit I-32100 Belluno Italy;
Univ Bologna Policlin S Orsola Malpighi Hosp Dept Med &
Surg Sci I-40138 Bologna Italy;
Univ Bologna Policlin S Orsola Malpighi Hosp Dept Med &
Surg Sci I-40138 Bologna Italy;
Indiana Univ Hlth Riley Hosp Children Indianapolis IN 46202 USA;
Indiana Univ Hlth Riley Hosp Children Indianapolis IN 46202 USA;
Univ Europea Madrid Hosp Univ Quiron Madrid Dept Pediat Neurol Madrid 28223 Spain;
Columbia Univ Dept Pathol &
Cell Biol Med Ctr New York NY 10032 USA;
Columbia Univ Dept Pediat Med Ctr New York NY 10032 USA;
Washington Univ Dept Pediat Div Genet &
Genom Med Sch Med St Louis MO 63110 USA;
Nationwide Childrens Hosp Inst Genom Med Columbus OH 43215 USA;
Nationwide Childrens Hosp Inst Genom Med Columbus OH 43215 USA;
Nationwide Childrens Hosp Inst Genom Med Columbus OH 43215 USA;
Nationwide Childrens Hosp Inst Genom Med Columbus OH 43215 USA;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Ist Super Sanita Dept Oncol &
Mol Med I-00161 Rome Italy;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Fdn IRCCS Casa Sollievo della Sofferenza Med Genet Div I-71013 San Giovanni Rotondo Italy;
Univ Hosp Magdeburg Inst Human Genet D-39120 Magdeburg Germany;
Univ Hosp Magdeburg Inst Human Genet D-39120 Magdeburg Germany;
Univ Cincinnati Dept Pediat Coll Med Cincinnati OH 45229 USA;
Vrije Univ Dept Clin Genet Amsterdam UMC NL-1117 Amsterdam Netherlands;
Univ Med Ctr Utrecht Dept Genet NL-3584 CX Utrecht Netherlands;
GeneDx Gaithersburg MD 20877 USA;
GeneDx Gaithersburg MD 20877 USA;
NimGenetics Med Dept Madrid 28049 Spain;
NimGenetics Med Dept Madrid 28049 Spain;
Fdn IRCCS Casa Sollievo della Sofferenza Med Genet Div I-71013 San Giovanni Rotondo Italy;
Osped San Bortolo Ambulatorio Genet Clin I-36100 Vicenza Italy;
Univ Cattolica Sacro Cuore Fdn Policlin Univ Gemelli Ctr Rare Dis &
Congenital Defects I-00168;
Univ Bologna Med Genet Unit Policlin S Orsola Malpighi I-40138 Bologna Italy;
Univ Bologna Med Genet Unit Policlin S Orsola Malpighi I-40138 Bologna Italy;
Icahn Sch Med Mt Sinai Mindich Child Hlth &
Dev Inst New York NY 10029 USA;
Univ Hosp Magdeburg Inst Human Genet D-39120 Magdeburg Germany;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
Univ Roma Tor Vergata Dept Chem Sci &
Technol I-00133 Rome Italy;
Univ Cincinnati Dept Pediat Coll Med Cincinnati OH 45229 USA;
Ist Super Sanita Dept Oncol &
Mol Med I-00161 Rome Italy;
Ist Super Sanita Dept Oncol &
Mol Med I-00161 Rome Italy;
Osped Pediat Bambino Gesu IRCCS Genet &
Rare Dis Res Div I-00146 Rome Italy;
机译:异常的HRAS转录物加工在Rasopathy临床光谱中产生了独特的表型
机译:异常的HRAS转录物加工在Rasopathy临床光谱中产生了独特的表型
机译:脆弱X综合征(FXS)和自闭症谱紊乱(ASD)的可见空间施工轨迹:神经开发条件下认知异质性的证据
机译:与神经塑性相关基因的失程赋予人类神经发育障碍的风险
机译:时间加工和神经发育障碍:从注意力缺陷/多动障碍,自闭症谱系障碍和22q11.2删除综合征的见解。
机译:增强型MAPK1功能导致Rasopathy临床光谱内的神经发育障碍
机译:增强型MAPK1功能导致Rasopathy临床光谱内的神经发育障碍
机译:自闭症谱系障碍成人认知增强疗法的随机临床试验。