Targeted Exome Sequencing Identifies Novel Mutations in Familial Myeloproliferative Neoplasms Patients in the State of Qatar

被引：0

作者：

Al-Dewik, Nader I. ^{[1
]}

Cassinat, Bruno ^{[2
]}

Kiladjian, Jean-Jacques ^{[2
,3
]}

Knuth, Alexander ^{[1
]}

Yassin, Mohamed A. ^{[4
]}

机构：

[1] HMC, Doha, Qatar

[2] Hop St Louis, Paris, France

[3] Univ Paris Diderot, Paris, France

[4] Hamad Med Corp, Natl Ctr Canc Care & Res, Doha, Qatar

来源：

BLOOD | 2014年 / 124卷 / 21期

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页数：3

共 50 条

[41] Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families
Yang, Liping
Yin, Xiaobei
Wu, Lemeng
Chen, Ningning
Zhang, Huirong
Li, Genlin
Ma, Zhizhong
BMJ OPEN, 2013, 3 (11):
[42] SURVIVAL IN PATIENTS WITH FAMILIAL AND SPORADIC MYELOPROLIFERATIVE NEOPLASMS
Hultcrantz, M.
Lund, S. H.
Landgren, O.
Samuelsson, J.
Goldin, L.
Oddson, A.
Bjorkholm, M.
Kristinsson, S. Y.
HAEMATOLOGICA, 2014, 99 : 128 - 128
[43] Survival in patients with familial and sporadic myeloproliferative neoplasms
Hultcrantz, Malin
Lund, Sigrun H.
Landgren, Ola
Samuelsson, Jan
Goldin, Lynn R.
Oddsson, Asmundur
Bjorkholm, Magnus
Kristinsson, Sigurdur Y.
BLOOD, 2015, 125 (23) : 3665 - 3666
[44] Whole exome sequencing identifies novel TRIOBP mutations as a cause of a distinct audiological manifestation
Pollak, A.
Lechowicz, U.
Pienkowski, V. A. Murcia
Stawinski, P.
Kosinska, J.
Skarzynski, H.
Oldak, M.
Ploski, R.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 847 - 847
[45] Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease
Gunadi, Kristy
Kalim, Alvin Santoso
Iskandar, Kristy
Marcellus, Rizki
Puspitarani, Dyah Ayu
Diposarosa, Rizki
Makhmudi, Akhmad
Astuti, Galuh Dyah Nur
JOURNAL OF PEDIATRIC SURGERY, 2023, 58 (04) : 723 - 728
[46] Whole-exome and targeted gene sequencing of gallbladder carcinoma identifies recurrent mutations in the ErbB pathway
Maolan Li
Zhou Zhang
Xiaoguang Li
Junyi Ye
Xiangsong Wu
Zhujun Tan
Chang Liu
Baiyong Shen
Xu-An Wang
Wenguang Wu
Daizhan Zhou
Di Zhang
Ting Wang
Bingya Liu
Kai Qu
Qichen Ding
Hao Weng
Qian Ding
Jiasheng Mu
Yijun Shu
Runfa Bao
Yang Cao
Peizhan Chen
Tianyu Liu
Lin Jiang
Yunping Hu
Ping Dong
Jun Gu
Wei Lu
Weibin Shi
Jianhua Lu
Wei Gong
Zhaohui Tang
Yong Zhang
Xuefeng Wang
Y Eugene Chin
Xiaoling Weng
Hong Zhang
Wei Tang
Yonglan Zheng
Lin He
Hui Wang
Yun Liu
Yingbin Liu
Nature Genetics, 2014, 46 : 872 - 876
[47] Whole-exome and targeted gene sequencing of gallbladder carcinoma identifies recurrent mutations in the ErbB pathway
Li, Maolan
Zhang, Zhou
Li, Xiaoguang
Ye, Junyi
Wu, Xiangsong
Tan, Zhujun
Liu, Chang
Shen, Baiyong
Wang, Xu-An
Wu, Wenguang
Zhou, Daizhan
Zhang, Di
Wang, Ting
Liu, Bingya
Qu, Kai
Ding, Qichen
Weng, Hao
Ding, Qian
Mu, Jiasheng
Shu, Yijun
Bao, Runfa
Cao, Yang
Chen, Peizhan
Liu, Tianyu
Jiang, Lin
Hu, Yunping
Dong, Ping
Gu, Jun
Lu, Wei
Shi, Weibin
Lu, Jianhua
Gong, Wei
Tang, Zhaohui
Zhang, Yong
Wang, Xuefeng
Chin, Y. Eugene
Weng, Xiaoling
Zhang, Hong
Tang, Wei
Zheng, Yonglan
He, Lin
Wang, Hui
Liu, Yun
Liu, Yingbin
NATURE GENETICS, 2014, 46 (08) : 872 - 876
[48] Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera
Elina A. M. Hirvonen
Esa Pitkänen
Kari Hemminki
Lauri A. Aaltonen
Outi Kilpivaara
Human Genomics, 11
[49] Familial Ebstein's anomaly: whole exome sequencing identifies novel phenotype associated with FLNA
Mercer, C. L.
Andreoeltti, G.
Carroll, A.
Salmon, A. P.
Temple, I. K.
Ennis, S.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 270 - 271
[50] Whole-exome sequencing identifies novel candidate predisposition genes for familial polycythemia vera
Hirvonen, Elina A. M.
Pitkanen, Esa
Hemminki, Kari
Aaltonen, Lauri A.
Kilpivaara, Outi
HUMAN GENOMICS, 2017, 11

← 1 2 3 4 5 →