These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. [Clinical phenotype and genetic analysis of a Chinese patient featuring X-linked Claes-Jensen type syndromic mental retardation]. Gao M, Xing M, Zhang K, Lyu Y, Ma J, Gai Z, Liu Y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul 10; 37(7):736-738. PubMed ID: 32619253 [Abstract] [Full Text] [Related]
4. [Clinical and genetic analysis of a child with X-linked intellectual developmental disorder due to a novel variant of NEXMIF gene]. Li Z, Liu K, Zhao X, Li L. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jul 10; 41(7):821-824. PubMed ID: 38946365 [Abstract] [Full Text] [Related]
8. [X-linked mental retardation combined with autism caused by a novel hemizygous mutation of GRIA3 gene]. Bai Z, Kong X. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Aug 10; 36(8):829-833. PubMed ID: 31400139 [Abstract] [Full Text] [Related]
9. [Analysis of ARID1B gene variant in a patient with mental retardation and ejaculatory dysfunction]. Shi R, Xu Y, Zhang J, Chang Y, Liao W, Wang H. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Sep 10; 40(9):1146-1149. PubMed ID: 37643963 [Abstract] [Full Text] [Related]
10. [Analysis of CNNM2 gene variant in a child with Hypomagnesemia, seizures, and mental retardation syndrome]. Wang L, Zhang H, Luo J, Qi F, Liu Y, Zhang K, Gao Z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Aug 10; 40(8):1004-1008. PubMed ID: 37532502 [Abstract] [Full Text] [Related]
13. [Identification of a c.1A>G initial codon variation of ARX gene in a child with severe mental retardation]. Shen X, Qi F, Gu C. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Feb 10; 37(2):131-134. PubMed ID: 32034737 [Abstract] [Full Text] [Related]
17. Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability. Ibarluzea N, Hoz AB, Villate O, Llano I, Ocio I, Martí I, Guitart M, Gabau E, Andrade F, Gener B, Tejada MI. Genes (Basel); 2020 Jan 02; 11(1):. PubMed ID: 31906484 [Abstract] [Full Text] [Related]
19. [Clinical and genetic analysis of three children with Menkes disease due to variants of ATP7A gene]. Wang Z, Chen Q, Wang Y, Liu L, Li C. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Jun 10; 40(6):668-673. PubMed ID: 37212000 [Abstract] [Full Text] [Related]
20. [Analysis of a patient with X-linked mental retardation by next generation sequencing]. Lyu Y, Yang Y, Liu Y, Gai Z. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):257-260. PubMed ID: 29653005 [Abstract] [Full Text] [Related] Page: [Next] [New Search]