Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Microcephaly and ASPM[original query] |
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Investigation of MCPH1 G37995C and ASPM A44871G polymorphisms and brain size in a healthy cohort. NeuroImage 2007 Aug 37 (2): 394-400. Dobson-Stone C, Gatt J M, Kuan S A, Grieve S M, Gordon E, Williams L M, Schofield P |
A common SNP of MCPH1 is associated with cranial volume variation in Chinese population. Human molecular genetics 2008 May 17 (9): 1329-35. Wang Jin-kai, Li Yi, Su Bi |
Sex-dependent association of common variants of microcephaly genes with brain structure. Proceedings of the National Academy of Sciences of the United States of America 2010 Jan 107 (1): 384-8. Rimol Lars M, Agartz Ingrid, Djurovic Srdjan, Brown Andrew A, Roddey J Cooper, Kähler Anna K, Mattingsdal Morten, Athanasiu Lavinia, Joyner Alexander H, Schork Nicholas J, Halgren Eric, Sundet Kjetil, Melle Ingrid, Dale Anders M, Andreassen Ole A, |
Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders. Psychiatric genetics 2014 Oct 24 (5): 191-200. Stein Catherine M, Truitt Barbara, Deng Fenghua, Ciesla Allison Avrich, Qiu Feiyou, Joseph Peronne, Raghavendra Rekha, Fondran Jeremy, Igo Robert P, Tag Jessica, Freebairn Lisa, Taylor H Gerry, Lewis Barbara A, Iyengar Sudha |
Molecular genetics of human primary microcephaly: an overview. BMC medical genomics 2015 8 Suppl 1 S4. Faheem Muhammad, Naseer Muhammad Imran, Rasool Mahmood, Chaudhary Adeel G, Kumosani Taha A, Ilyas Asad Muhammad, Pushparaj Peter, Ahmed Farid, Algahtani Hussain A, Al-Qahtani Mohammad H, Saleh Jamal Has |
Updates on Clinical and Genetic Heterogeneity of ASPM in 12 Autosomal Recessive Primary Microcephaly Families in Pakistani Population. Frontiers in pediatrics 2021 7 9 695133. Khan Niaz Muhammad, Hussain Basharat, Zheng Chenqing, Khan Ayaz, Masoud Muhammad Shareef, Gu Qingquan, Qiu Linhui, Malik Naveed Altaf, Qasim Muhammad, Tariq Muhammad, Chang Junl |
Molecular Genetic Analysis of Newborns with Congenital Microcephaly. Neonatology 2022 Jun 1-9. Ye Chang, Mei Hongfang, Chen Huiyao, Dong Xinran, Lu Yulan, Wu Bingbing, Wang Huijun, Hu Liyuan, Cheng Guoqiang, Zhou Wenhao, Yang L |
Novel and recurrent ASPM mutations of founder effect in Chinese population. Brain & development 2022 Apr . Li Mengting, Luo Jingrong, Yang Qi, Chen Fei, Chen Jie, Qin Jiayi, He Wei, Chen Junjie, Yi Sheng, Qin Zailong, Yi Shang, Huang Limei, Qiu Xiaoxia, Pan Pingshan, Luo Jingsi, Shen Yipi |
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- Page last updated:Apr 16, 2024
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