首页> 外文OA文献 >VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans

【2h】

VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans

机译：VAX1突变与微蛋白，语料库胼um患者和口腔上的突变：人类中vax1表型的第一个描述

代理获取

本网站仅为用户提供外文OA文献查询和代理获取服务，本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文，但由于OA文献来源多样且变更频繁，仍可能出现获取不到、文献不完整或与标题不符等情况，如果获取不到我们将提供退款服务。请知悉。

页面导航

著录项
引文网络
相似文献
相关主题

著录项

作者
Anne M. Slavotinek; Ryan Chao; Tomas Vacik; Mani Yahyavi; Hana Abouzeid; Tanya Bardakjian; Adele Schneider; Gary Shaw; Elliott H. Sherr; Greg Lemke; Mohammed Youssef; Daniel F. Schorderet;
展开▼
作者单位

展开▼
年度 2011
总页数
原文格式 PDF
正文语种
中图分类

相似文献

外文文献
中文文献
专利

1. VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans [J] . SlavotinekA.M., ChaoR., VacikT., Human mutation . 2012,第2期

机译：与小眼症，call体发育不全和口面部裂伤相关的VAX1突变：人类中VAX1表型的第一个描述
2. Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. - Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele [J] . Schoner Katharina, Kohlhase Juergen, Mueller Annette M., Prenatal Diagnosis . 2013,第Null期

机译：脑积水，call体发育不全和唇裂/ pal裂代表胎儿中经常伴有彼得斯氏综合征和B3GALTL突变。 -胎儿PPS表型，由丹迪·沃克囊肿和脑膨出扩大
3. Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. - Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele [J] . Schoner Katharina, Kohlhase Juergen, Mueller Annette M., Prenatal Diagnosis . 2013,第Null期

机译：脑积水，胼callosum的验血和裂隙唇/腭，代表胎儿与Peters Plus综合征和B3GALTL突变的频繁关联。 - 胎儿PPS表型，由Dandy Walker Cyst和Encephalocele扩展
4. Shape Preservation Based on Gaussian Radial Basis Function Interpolation on Human Corpus Callosum [C] . Umut Orcun Turgut, Didem Gokcay Spectral and shape analysis in medical imaging . 2016

机译：基于高斯径向基函数插值的人Corp体形状保持
5. Social Inferences from Animations in Agenesis of the Corpus Callosum: Labeled Topic Modeling [D] . Renteria-Vazquez, Tiffany A. 2019

机译：Call体再生中动画的社会推理：标记主题建模
6. Brief Report: VAX1 mutation associated with microphthalmia corpus callosum agenesis and orofacial clefting – the first description of a VAX1 phenotype in humans [O] . Anne M. Slavotinek, Ryan Chao, Tomas Vacik, -1

机译：简要介绍：VAX1突变与微蛋白语料库胼um患者和口腔细胞 - 人类中的VAX1表型的第一个描述
7. Molecular Screening of VAX1 Gene Polymorphisms Uncovered the Genetic Heterogeneity of Nonsyndromic Orofacial Cleft Among Saudi Arabian Patients [O] . Heba Jafar Sabbagh, Nicola P.T. Innes, Sherif Edris Ahmed, 2019

机译：vax1基因多态性的分子筛发现了沙特阿拉伯患者中非肌瘤肉体裂缝的遗传异质性

VAX1 mutation associated with microphthalmia, corpus callosum agenesis, and orofacial clefting: The first description of a VAX1 phenotype in humans

著录项

引文网络

相似文献

相关主题

期刊订阅