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在“Elsevier电子期刊”中，命中：784条，耗时：0.0490094 秒

在所有数据库中总计命中：1,819条

1.Sequencing and comparative analyses of Aegilops tauschii chromosome arm 3DS reveal rapid evolution of Triticeae genomes

作者：Jingzhong Xie^a ; ¹ ; Naxin Huo^b ; ^c ; ¹ ; Shenghui Zhou^a ; ¹ ; Yi Wang^b ; ¹ ; Guanghao Guo^a ; Karin R. Deal^c ; Shuhong Ouyang^a ; Yong Liang^a ; Zhenzhong Wang^a ; Lichan Xiao^c ; Tingting Zhu^c ; Tiezhu Hu^b ; Vijay Tiwari^d ; Jianwei Zhang^e ; Hongxia Li^b ; Zhongfu Ni^a ; Yingyin Yao^a ; Huiru Peng^a ; Shengli Zhang^b ; Olin D. Anderson^b ; Patrick E. McGuire^c ; Jan Dvorak^c ; ^{jdvorak@ucdavis.edu} ; Ming-Cheng Luo^c ; ^{mcluo@ucdavis.edu} ; Zhiyong Liu^a ; ^{zyliu@genetics.ac.cn} ; Yong Q. Gu^b ; ^{yong.gu@ars.usda.gov} ; Qixin Sun^a ; ^{qxsun@cau.edu.cn}

关键词：Aegilops tauschii ; Genome sequencing ; Sequence assembly ; Comparative genomics ; Grass evolution

刊名：Journal of Genetics and Genomics

出版年：2017

2.Zinc deficiency reduces fertility in C. elegans hermaphrodites and disrupts oogenesis and meiotic progression

作者：James Hester^a ; Wendy Hanna-Rose^b ; Francisco Diaz^a ; ^c ; ^{fjd10@psu.edu}

关键词：Zinc ; C. elegans ; Oogenesis ; Fertility

刊名：Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology

出版年：2017

3.Moyamoya syndrome and 6p chromosome rearrangements: Expanding evidences of a new association

关键词：Moyamoya syndrome ; Pediatric stroke ; Transient ischemic attack ; Chromosome rearrangement ; Short arm chromosome 6

刊名：European Journal of Paediatric Neurology

出版年：2016

4.Rare interstitial deletion of chromosome 2p11.2p12. Report of a new patient with developmental delay and unusual clinical features

作者：Rosamaria Silipigni^a ; ^{rosamariasilipigni@gmail.com" class="auth_mail" title="E-mail the corresponding author} ; Elisa Cattaneo^b ; Marco Baccarin^a ; Monica Fumagalli^c ; Maria Francesca Bedeschi^b

关键词：Deletion 2p11.2p12 ; CGH array ; Bilateral choanal atresia ; Atrial septal defect ; Developmental delay ; Facial anomalies ; CTNNA2 ; LRRTM1 ; REEP1

刊名：European Journal of Medical Genetics

出版年：2016

5.Cloning of the ω-secalin gene family in a wheat 1BL/1RS translocation line using BAC clone sequencing

作者：Meng Jun Li ^{lmj199612@aliyun.com" class="auth_mail" title="E-mail the corresponding author} ; Ya Qing Li ^{liyaqing2002@126.com" class="auth_mail" title="E-mail the corresponding author} ; Nan Zhang ^{zhangnan-89@163.com" class="auth_mail" title="E-mail the corresponding author} ; Zhan Liang Shi ; ^{shizhanl@tom.com" class="auth_mail" title="E-mail the corresponding author}

关键词：Bacterial artificial chromosome (BAC) ; Wheat ; ω-Secalin ; 1BL/1RS translocation line

刊名：Electronic Journal of Biotechnology

出版年：2016

6.Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement

作者：Egle Preiksaitiene ; ^{egle.preiksaitiene@mf.vu.lt" class="auth_mail" title="E-mail the corresponding author} ; Eglė Benu&scaron ; ienė ; Zivile Ciuladaite ; Vytautas &Scaron ; liužas ; Violeta Mik&scaron ; tienė ; Vaidutis Kučinskas

关键词：neural tube defects ; 3q26.1-qter duplication ; 5p13.33-pter deletion

刊名：Taiwanese Journal of Obstetrics and Gynecology

出版年：2016

7.Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosis

作者：Francesco Libotte^a ; Domenico Bizzoco^a ; Ivan Gabrielli^a ; Alvaro Mesoraca^a ; Pietro Cignini^b ; Salvatore Giovanni Vitale^c ; ^{vitalesalvatore@hotmail.com} ; Ilaria Marilli^d ; Ferdinando Antonio Gulino^d ; Agnese Maria Chiara Rapisarda^d ; Claudio Giorlandino^b

关键词：cytogenetic analysis ; isochromosome 12p ; Pallister&ndash ; Killian syndrome ; prenatal diagnosis ; tetrasomy 12p

刊名：Taiwanese Journal of Obstetrics and Gynecology

出版年：2016

8.Dosage compensation and nuclear organization: cluster to control chromosome-wide gene expression

作者：Rahul Sharma¹ ; ² ; Peter Meister¹ ; ^{peter.meister@izb.unibe.ch" class="auth_mail" title="E-mail the corresponding author}

刊名：Current Opinion in Genetics & Development

出版年：2016

9.Novel WASP mutation in a patient with Wiskott-Aldrich syndrome: Case report and review of the literature

作者：M. Eghbali^a ; M. Sadeghi-Shabestari^b ; F. Najmi Varzaneh^c ; ^d ; A. Zare Bidoki^c ; N. Rezaei^a ; ^c ; ^d ; ^{rezaei_nima@tums.ac.ir" class="auth_mail" title="E-mail the corresponding author}

关键词：Eczema ; Recurrent infection ; Thrombocytopenia ; Novel mutation ; Wiskott&ndash ; Aldrich syndrome

刊名：Allergologia et Immunopathologia

出版年：2016

10.A new familial case of microdeletion syndrome 10p15.3

作者：Marlene Eggert^a ; ^{Marlene.Eggert@med.uni-muenchen.de" class="auth_mail" title="E-mail the corresponding author} ; Stefan Mü ; ller^a ; Uwe Heinrich^b ; Yasmin Mehraein^a

关键词：Microdeletion ; 10p15.3 syndrome ; Language disorder

刊名：European Journal of Medical Genetics

出版年：2016

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