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De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine

机译：XP11.3的De Novo微缺失仅包括单氨基氧化酶A和B基因，患有发作性婴儿的婴幼儿：个性化医学的基因组学方法

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Ryan E. O’Leary; Jean C. Shih; Keith Hyland; Nancy Kramer; Y. Jane Tavyev Asher; John M. Graham;
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年度 2012
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1. De novo 19p13.2 microdeletion encompassing the insulin receptor and resistin genes in a patient with obesity and learning disability [J] . WangensteenT., Retterst?lL., R?dningenO.K., American journal of medical genetics, Part A . 2013,第6期

机译：肥胖和学习障碍患者的从头19p13.2微缺失涉及胰岛素受体和抵抗素基因
2. Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome [J] . Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Taiwanese journal of obstetrics and gynecology . 2017,第2期

机译：家族性Xp22.33基因微缺失的分子细胞遗传学特征和产前诊断，其在男性胎儿中具有矮小同源盒基因，且预后良好
3. Evidence for interplay between genes and parenting on infant temperament in the first year of life: Monoamine oxidase A polymorphism moderates effects of maternal sensitivity on infant anger proneness [J] . PicklesA., HillJ., BreenG., Journal of child psychology and psychiatry . 2013,第12期

机译：基因和育儿对婴儿气质的相互作用的证据：单胺氧化酶A多态性可减轻母体敏感性对婴儿愤怒倾向的影响
4. De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine [O] . Ryan E. O’Leary, Jean C. Shih, Keith Hyland, -1

机译：XP11.3的De Novo微缺失仅包括单氨基氧化酶A和B基因患有发作性婴儿的婴幼儿：个性化医学的基因组学方法
5. Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome [O] . Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, 2017

机译：家族性Xp22.33微缺失的分子细胞遗传学表征和产前诊断，包括小胎儿的身材矮小的同源框基因，结果良好

De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine

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