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机译:FGF9突变导致颅骨衰竭和多个同义症
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Department of Biochemistry and Molecular BiologyRosalind Franklin University of Medicine and;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Department of Biochemistry and Molecular BiologyRosalind Franklin University of Medicine and;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
Institute of Medical &
Molecular Genetics (INGEMM)Hospital Universitario La Paz Universidad Aut;
bone; craniosynostosis; FGF9; skeletal dysplasia; suture;
机译:FGF9突变导致颅骨衰竭和多个同义症
机译:一种新型GDF6突变的多发性鼻窦综合症的家庭,没有听力损失。
机译:一种具有多个同义术综合征的家庭中的一种新的GDF6突变,没有听力损失
机译:FGFR3 P250R突变是冠状颅骨愈伤症中增加的重新进效率的标志物
机译:用于确定多发性硬化样突变对髓鞘碱性蛋白的影响的生物物理方法。
机译:多发性骨糖综合症是由于FGF9基因第2外显子的错义突变。
机译:FGF9中的一个点突变阻碍了关节突突形成,导致多个同义症综合征