Human Genome Epidemiology Literature Finder
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Query Trace: Counseling and PEX1[original query] |
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Expanding the clinical and genetic spectrum of Heimler syndrome. Orphanet journal of rare diseases 2019 12 14 (1): 290. Gao Feng-Juan, Hu Fang-Yuan, Xu Ping, Qi Yu-He, Li Jian-Kang, Zhang Yong-Jin, Chen Fang, Chang Qing, Song Fang, Shen Si-Mai, Xu Ge-Zhi, Wu Ji-Ho |
First-line exome sequencing in Palestinian and Israeli Arabs with neurological disorders is efficient and facilitates disease gene discovery. European journal of human genetics : EJHG 2020 Mar . Hengel Holger, Buchert Rebecca, Sturm Marc, Haack Tobias B, Schelling Yvonne, Mahajnah Muhammad, Sharkia Rajech, Azem Abdussalam, Balousha Ghassan, Ghanem Zaid, Falana Mohammed, Balousha Osama, Ayesh Suhail, Keimer Reinhard, Deigendesch Werner, Zaidan Jimmy, Marzouqa Hiyam, Bauer Peter, Schöls Ludg |
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