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941.
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942.
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Targeted Next-Generation Sequencing Is a Sensitive Tool for Differential Diagnosis of Myelodysplastic Syndromes in Bone Marrow Trephines. [electronic resource] by
- Bräuninger, Andreas
- Blau, Wolfgang
- Kunze, Kristin
- Desch, Ann-Kathrin
- Brobeil, Alexander
- Tur, Mehmet K
- Etschmann, Benjamin
- Günther, Ulrich
- Körholz, Dieter
- Schliesser, Georg
- Käbisch, Andreas
- Kiehl, Michael
- Rummel, Mathias
- Gattenlöhner, Stefan
Producer: 20190916
In:
The Journal of molecular diagnostics : JMD vol. 20
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943.
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944.
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Microevolution of Neisseria lactamica during nasopharyngeal colonisation induced by controlled human infection. [electronic resource] by
- Pandey, Anish
- Cleary, David W
- Laver, Jay R
- Gorringe, Andrew
- Deasy, Alice M
- Dale, Adam P
- Morris, Paul D
- Didelot, Xavier
- Maiden, Martin C J
- Read, Robert C
Producer: 20190422
In:
Nature communications vol. 9
Availability: No items available.
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945.
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[Assessment on Application of 24 Y-STR Loci in Forensic Science]. [electronic resource] by
- L, M
- Huang, L
- Wang, X J
- Chen, Y L
- Sheng, X
- Li, Y N
- Bao, Y
- Jiang, L
- Zhu, R X
- Xu, Q N
- Zhang, J S
- Li, C T
- Bian, Y N
Producer: 20181015
In:
Fa yi xue za zhi vol. 34
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946.
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947.
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948.
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949.
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950.
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951.
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[A standard protocol for detection of EGFR mutations in cytologic specimens]. [electronic resource] by
- Wang, Zheng
- Wu, Xiaonan
- Shi, Yuankai
- Han, Xiaohong
- Cheng, Gang
- Li, Lin
- Zhang, Li
- Zhang, Yuhui
- Mu, Xinlin
- Zhu, Guangqing
- Fan, Zaiwen
- Yang, Li
- Di, Jing
- Jia, Xinrui
- Liu, Dongge
Producer: 20150411
In:
Zhonghua zhong liu za zhi [Chinese journal of oncology] vol. 36
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952.
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953.
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TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia. [electronic resource] by
- Lattante, Serena
- Le Ber, Isabelle
- Camuzat, Agnès
- Dayan, Sarah
- Godard, Chloé
- Van Bortel, Inge
- De Septenville, Anne
- Ciura, Sorana
- Brice, Alexis
- Kabashi, Edor
Producer: 20140325
In:
Neurobiology of aging vol. 34
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954.
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Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. [electronic resource] by
- Spier, Isabel
- Drichel, Dmitriy
- Kerick, Martin
- Kirfel, Jutta
- Horpaopan, Sukanya
- Laner, Andreas
- Holzapfel, Stefanie
- Peters, Sophia
- Adam, Ronja
- Zhao, Bixiao
- Becker, Tim
- Lifton, Richard P
- Perner, Sven
- Hoffmann, Per
- Kristiansen, Glen
- Timmermann, Bernd
- Nöthen, Markus M
- Holinski-Feder, Elke
- Schweiger, Michal R
- Aretz, Stefan
Producer: 20160712
In:
Journal of medical genetics vol. 53
Availability: No items available.
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955.
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TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts. [electronic resource] by
- Le Ber, Isabelle
- De Septenville, Anne
- Millecamps, Stéphanie
- Camuzat, Agnès
- Caroppo, Paola
- Couratier, Philippe
- Blanc, Frédéric
- Lacomblez, Lucette
- Sellal, François
- Fleury, Marie-Céline
- Meininger, Vincent
- Cazeneuve, Cécile
- Clot, Fabienne
- Flabeau, Olivier
- LeGuern, Eric
- Brice, Alexis
Producer: 20160815
In:
Neurobiology of aging vol. 36
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956.
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957.
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958.
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High prevalence of W1282x mutation in cystic fibrosis patients from Karachay-Cherkessia. [electronic resource] by
- Petrova, N V
- Kashirskaya, N Yu
- Vasilyeva, T A
- Timkovskaya, E E
- Voronkova, A Yu
- Shabalova, L A
- Kondratyeva, E I
- Sherman, V D
- Novoselova, O G
- Kapranov, N I
- Zinchenko, R A
- Ginter, E K
- Makaov, A Kh-M
- Kerem, B
Producer: 20171218
In:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society vol. 15
Availability: No items available.
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959.
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960.
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