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Clinical manifestations of a sporadic maturity-onset diabetes of the young (MODY) 5 with a whole deletion of HNF1B based on 17q12 microdeletion. [electronic resource] by
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- Honoki, Hisae
- Iwata, Minoru
- Enkaku, Asako
- Takikawa, Akiko
- Kuwano, Takahide
- Watanabe, Yoshiyuki
- Nishimura, Ayumi
- Liu, Jianhui
- Chujo, Daisuke
- Fujisaka, Shiho
- Enya, Mayumi
- Horikawa, Yukio
- Tobe, Kazuyuki
Producer: 20200522
In:
Endocrine journal vol. 66
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Association of single nucleotide polymorphisms in TCF2 with type 2 diabetes susceptibility in a Han Chinese population. [electronic resource] by
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- Liu, An
- Xu, Lidan
- Sun, Donglin
- Jin, Yan
- Yu, Yang
- Meng, Xiangning
- Bai, Jing
- Chen, Feng
- Fu, Songbin
Producer: 20130624
In:
PloS one vol. 7
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264.
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Pancreatic Ductal Deletion of Hnf1b Disrupts Exocrine Homeostasis, Leads to Pancreatitis, and Facilitates Tumorigenesis. [electronic resource] by
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- Dirami, Thassadite
- Stedman, Aline
- De Vas, Matias
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- Cereghini, Silvia
- Morillon, Lucie
- Guerra, Carmen
- Couvelard, Anne
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- Haumaitre, Cécile
Producer: 20200720
In:
Cellular and molecular gastroenterology and hepatology vol. 8
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Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder. [electronic resource] by
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- Bunce, Benjamin
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- Waller, Simon
- Bowman, Pamela
- Ford, Tamsin
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Producer: 20171002
In:
Kidney international vol. 90
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ATARiS: computational quantification of gene suppression phenotypes from multisample RNAi screens. [electronic resource] by
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- Beroukhim, Rameen
- Garraway, Levi A
- Margolin, Adam A
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- Mesirov, Jill P
Producer: 20131017
In:
Genome research vol. 23
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276.
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Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family. [electronic resource] by
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- Chang, Shuenn-Dyh
- Wang, Tzu-Hao
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- Tsai, Jeng-Daw
- Liu, Yu-Peng
- Chern, Schu-Rern
- Wu, Peih-Shan
- Su, Jun-Wei
- Chen, Yu-Ting
- Wang, Wayseen
Producer: 20140930
In:
Taiwanese journal of obstetrics & gynecology vol. 52
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Association of I27L polymorphism of hepatocyte nuclear factor-1 alpha gene with high-density lipoprotein cholesterol level. [electronic resource] by
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- Ikegami, Hiroshi
- Fujisawa, Tomomi
- Nojima, Koji
- Itoi-Babaya, Michiko
- Inoue, Kaori
- Nakura, Jun
- Abe, Michiko
- Yamamoto, Miyuki
- Jin, Jin Ji
- Wu, Zhihong
- Miki, Tetsuro
- Fukuda, Masakatsu
- Ogihara, Toshio
Producer: 20030701
In:
The Journal of clinical endocrinology and metabolism vol. 88
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