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WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome.
Authors: Kim, Hyung-Goo; Ahn, Jang-Won; Kurth, Ingo; Ullmann, Reinhard; Kim, Hyun-Taek; Kulharya, Anita; Ha, Kyung-Soo; Itokawa, Yasuhide; Meliciani, Irene; Wolfgang Wenzel, Wolfgang Wenzel; Lee, Deresa; Rosenberger, Georg; Ozata, Metin; Bick, David P.; Sherins, Richard J.; Nagase, Takahiro; Tekin, Mustafa; Kim, Soo-Hyun; Kim, Cheol-Hee; Ropers, Hans-Hilger; Gusella, James F.; Kalscheuer, Vera M.; Choi, Cheol Yong; Layman, Lawrence C.
Date of Publication (YYYY-MM-DD): 2010-10-08
Title of Journal: American Society of Human Genetics
Volume: 87
Issue / Number: 4
Start Page: 465
End Page: 479
Document Type: Article
ID: 533112.0
 
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Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome.
Authors: Abo-Dalo, Benjamin; Kim, Hyung-Goo; Roes, Melanie; Stefanova, Margarita; Higgins, Anne; Shen, Yiping; Mundlos, Stefan; Quade, Bradley J.; Gusella, James F.; Kutsche, Kerstin
Date of Publication (YYYY-MM-DD): 2007-10-15
Title of Journal: American Journal of Medical Genetics / Part A
Volume: 143
Issue / Number: 22
Start Page: 2668
End Page: 2674
Document Type: Article
ID: 334846.0
 
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Entries: 1-2  
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