DE NOVO COPY NUMBER VARIANTS AND PARENTAL AGE

Graham J. M. Jr.; Wadharwan I; Foyouzi N.; Hai Y.; Guo X.; Rosenberg J.

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DE NOVO COPY NUMBER VARIANTS AND PARENTAL AGE

机译：de novo拷贝数变体和父母年龄

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来源
《American journal of medical genetics, Part A》 |2018年第6期|共2页
作者
Graham J. M. Jr.; Wadharwan I; Foyouzi N.; Hai Y.; Guo X.; Rosenberg J.;
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作者单位

Cedars Sinai Med Ctr Dept Pediat Div Med Genet Los Angeles CA 90048 USA;

Fortis Escorts Med Ctr Dept Obstet &

Gynecol Faridabad Haryana India;

Univ Calif Los Angeles Sch Med Dept Pediat Div Med Genet Los Angeles CA 90024 USA;

Harbor UCLA Med Ctr Los Angeles Biomed Res Inst Torrance CA 90509 USA;

Harbor UCLA Med Ctr Los Angeles Biomed Res Inst Torrance CA 90509 USA;

Baylor Coll Med Dept Mol &

Human Genet Houston TX 77030 USA;

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原文格式 PDF
正文语种 eng
中图分类医学遗传学;
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1. A de novo originated gene depresses budding yeast mating pathway and is repressed by the protein encoded by its antisense strand [J] . Dan Li, Yang Dong, Yu Jiang, 细胞研究：英文版 . 2010,第004期
2. DE NOVO COPY NUMBER VARIANTS AND PARENTAL AGE [J] . Graham J. M. Jr., Wadharwan I, Foyouzi N., American journal of medical genetics, Part A . 2018,第6期

机译：de novo拷贝数变体和父母年龄
3. De novo copy number variants associated with intellectual disability have a paternal origin and age bias. [J] . Hehir Kwa JY, Rodriguez Santiago B, Vissers LE, Journal of Medical Genetics . 2011,第11期

机译：与智力障碍相关的从头复制号码变体具有父系起源和年龄偏见。
4. Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia [J] . Martin Andrew K., Robinson Gail, Reutens David, American journal of medical genetics, Part B. Neuropsychiatric genetics: the official publication of the International Society of Psychiatric Genetics . 2015,第5期

机译：精神分裂症患者罕见拷贝数变异负担的临床和父母年龄特征
5. Constrained variant detection with SPaRC: Sparsity, parental relatedness, and coverage [C] . Mario Banuelos, Rubi Almanza, Lasith Adhikari, Annual International Conference of the IEEE Engineering in Medicine and Biology Society . 2016

机译：SPaRC的受限变体检测：稀疏性，父母亲相关性和覆盖率
6. De novo design of metalloproteins with variant hydrophobic cores [D] . Xie, Fei. 2009

机译：从头开始设计具有变异疏水核心的金属蛋白
7. Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria [O] . Samin A. Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, 2013

机译：稀有和从头复制数目变体在Call体发育不全中普遍存在但在小脑发育不全或多发性小体质性生殖中并不普遍。
8. Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria. [O] . Samin A Sajan, Liliana Fernandez, Sahar Esmaeeli Nieh, 2013

机译：稀有和从头拷贝数变体在胼call体发育不全中普遍存在，但在小脑发育不全或多发性微血管中不常见。

DE NOVO COPY NUMBER VARIANTS AND PARENTAL AGE

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