日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Increasing the yield in targeted next-generation sequencing by implicating CNV analysis, non-coding exons and the overall variant load: the example of retinal dystrophies

通过引入拷贝数变异分析、非编码外显子和总体变异负荷来提高靶向二代测序的产量:以视网膜营养不良为例

Eisenberger, Tobias; Neuhaus, Christine; Khan, Arif O; Decker, Christian; Preising, Markus N; Friedburg, Christoph; Bieg, Anika; Gliem, Martin; Charbel Issa, Peter; Holz, Frank G; Baig, Shahid M; Hellenbroich, Yorck; Galvez, Alberto; Platzer, Konrad; Wollnik, Bernd; Laddach, Nadja; Ghaffari, Saeed Reza; Rafati, Maryam; Botzenhart, Elke; Tinschert, Sigrid; Börger, Doris; Bohring, Axel; Schreml, Julia; Körtge-Jung, Stefani; Schell-Apacik, Chayim; Bakur, Khadijah; Al-Aama, Jumana Y; Neuhann, Teresa; Herkenrath, Peter; Nürnberg, Gudrun; Nürnberg, Peter; Davis, John S; Gal, Andreas; Bergmann, Carsten; Lorenz, Birgit; Bolz, Hanno J

Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly

SIX3 和 SHH 基因的杂合突变与裂脑畸形相关,并进一步扩展了全前脑畸形的临床谱。

Hehr, Ute; Pineda-Alvarez, Daniel E; Uyanik, Goekhan; Hu, Ping; Zhou, Nan; Hehr, Andreas; Schell-Apacik, Chayim; Altus, Carola; Daumer-Haas, Cornelia; Meiner, Annechristin; Steuernagel, Peter; Roessler, Erich; Winkler, Juergen; Muenke, Maximilian

Multiplex-FISH for pre- and postnatal diagnostic applications

用于产前和产后诊断的多重FISH技术

Uhrig, S; Schuffenhauer, S; Fauth, C; Wirtz, A; Daumer-Haas, C; Apacik, C; Cohen, M; Müller-Navia, J; Cremer, T; Murken, J; Speicher, M R