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.
276 related articles for article (PubMed ID: 36039580)
1. Zeng W; Li J; Wang X; Jiang F; Men M Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2022 Jul; 47(7):847-857. PubMed ID: 36039580 [TBL] [Abstract][Full Text] [Related]
2. Expanding the mutational spectrum of monogenic hypogonadotropic hypogonadism: novel mutations in ANOS1 and FGFR1 genes. Gach A; Pinkier I; Szarras-Czapnik M; Sakowicz A; Jakubowski L Reprod Biol Endocrinol; 2020 Jan; 18(1):8. PubMed ID: 31996231 [TBL] [Abstract][Full Text] [Related]
3. Expanding the genetic spectrum of ANOS1 mutations in patients with congenital hypogonadotropic hypogonadism. Gonçalves CI; Fonseca F; Borges T; Cunha F; Lemos MC Hum Reprod; 2017 Mar; 32(3):704-711. PubMed ID: 28122887 [TBL] [Abstract][Full Text] [Related]
4. GnRH Deficient Patients With Congenital Hypogonadotropic Hypogonadism: Novel Genetic Findings in Neocleous V; Fanis P; Toumba M; Tanteles GA; Schiza M; Cinarli F; Nicolaides NC; Oulas A; Spyrou GM; Mantzoros CS; Vlachakis D; Skordis N; Phylactou LA Front Endocrinol (Lausanne); 2020; 11():626. PubMed ID: 32982993 [No Abstract] [Full Text] [Related]
5. Correlations Among Genotype and Outcome in Chinese Male Patients With Congenital Hypogonadotropic Hypogonadism Under HCG Treatment. Chen Y; Sun T; Niu Y; Wang D; Xiong Z; Li C; Liu K; Qiu Y; Sun Y; Gong J; Wang T; Wang S; Xu H; Liu J J Sex Med; 2020 Apr; 17(4):645-657. PubMed ID: 32171629 [TBL] [Abstract][Full Text] [Related]
6. Congenital Hypogonadotropic Hypogonadism with Anosmia and Gorlin Features Caused by a PTCH1 Mutation Reveals a New Candidate Gene for Kallmann Syndrome. Barraud S; Delemer B; Poirsier-Violle C; Bouligand J; Mérol JC; Grange F; Higel-Chaufour B; Decoudier B; Zalzali M; Dwyer AA; Acierno JS; Pitteloud N; Millar RP; Young J Neuroendocrinology; 2021; 111(1-2):99-114. PubMed ID: 32074614 [TBL] [Abstract][Full Text] [Related]
8. Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism. Hou Q; Wu J; Zhao Y; Wang X; Jiang F; Chen DN; Zheng R; Men M; Li JD Eur J Endocrinol; 2020 Sep; 183(3):245-254. PubMed ID: 32520725 [TBL] [Abstract][Full Text] [Related]
9. Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with Nie M; Xu H; Chen R; Mao J; Wang X; Xiong S; Zheng J; Yu B; Cui M; Ma W; Huang Q; Zhang H; Wu X Eur J Endocrinol; 2017 Oct; 177(4):389-398. PubMed ID: 28780519 [TBL] [Abstract][Full Text] [Related]
10. Classification of Sun B; Wang X; Mao J; Zhao Z; Zhang W; Nie M; Wu X Front Genet; 2021; 12():770680. PubMed ID: 35047002 [No Abstract] [Full Text] [Related]
11. Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism. Aoyama K; Mizuno H; Tanaka T; Togawa T; Negishi Y; Ohashi K; Hori I; Izawa M; Hamajima T; Saitoh S J Pediatr Endocrinol Metab; 2017 Oct; 30(10):1111-1118. PubMed ID: 28915117 [TBL] [Abstract][Full Text] [Related]
12. A novel splice site variant in ANOS1 gene leads to Kallmann syndrome in three siblings. Jiang X; Li D; Gao Y; Zhang X; Wang X; Yang Y; Shen Y Gene; 2020 Feb; 726():144177. PubMed ID: 31669640 [TBL] [Abstract][Full Text] [Related]
13. Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1. Chu G; Li P; Zhao Q; He R; Zhao Y Reprod Biol Endocrinol; 2023 Mar; 21(1):23. PubMed ID: 36859276 [TBL] [Abstract][Full Text] [Related]
14. Genetic Profiles and Three-year Follow-up Study of Chinese Males With Congenital Hypogonadotropic Hypogonadism. Zhang L; Gao Y; Du Q; Liu L; Li Y; Dey SK; Banerjee S; Liao Z J Sex Med; 2021 Sep; 18(9):1500-1510. PubMed ID: 34348883 [TBL] [Abstract][Full Text] [Related]
15. Correlation Analysis of Genotypes and Phenotypes in Chinese Male Pediatric Patients With Congenital Hypogonadotropic Hypogonadism. Wang Y; Qin M; Fan L; Gong C Front Endocrinol (Lausanne); 2022; 13():846801. PubMed ID: 35669683 [TBL] [Abstract][Full Text] [Related]
17. Genetic architecture of congenital hypogonadotropic hypogonadism: insights from analysis of a Portuguese cohort. Carriço JN; Gonçalves CI; Al-Naama A; Syed N; Aragüés JM; Bastos M; Fonseca F; Borges T; Pereira BD; Pignatelli D; Carvalho D; Cunha F; Saavedra A; Rodrigues E; Saraiva J; Ruas L; Vicente N; Martin Martins J; De Sousa Lages A; Oliveira MJ; Castro-Correia C; Melo M; Martins RG; Couto J; Moreno C; Martins D; Oliveira P; Martins T; Martins SA; Marques O; Meireles C; Garrão A; Nogueira C; Baptista C; Gama-de-Sousa S; Amaral C; Martinho M; Limbert C; Barros L; Vieira IH; Sabino T; Saraiva LR; Lemos MC Hum Reprod Open; 2024; 2024(3):hoae053. PubMed ID: 39308770 [TBL] [Abstract][Full Text] [Related]
18. A Novel Noncanonical Splicing Mutation of ANOS1 Gene in Siblings with Kallmann Syndrome Identified by Whole-Exome Sequencing. Xia Y; Guo H; Ge H; Feng K; Qu X; Wan F; Zhang C; Yang J Reprod Sci; 2022 Feb; 29(2):475-479. PubMed ID: 34231177 [TBL] [Abstract][Full Text] [Related]
19. Mutation spectrum and frequency of copy number variations of the ANOS1 gene in patients with Kallmann syndrome or normosmic isolated hypogonadotropic hypogonadism. Hye Kim J; Choi Y; Hwang S; Yoon JH; Lee J; Jae Kang M; Kim GH; Yoo HW; Choi JH Endocr Connect; 2023 May; 12(5):. PubMed ID: 36917044 [TBL] [Abstract][Full Text] [Related]
20. New genetic findings in a large cohort of congenital hypogonadotropic hypogonadism. Amato LGL; Montenegro LR; Lerario AM; Jorge AAL; Guerra Junior G; Schnoll C; Renck AC; Trarbach EB; Costa EMF; Mendonca BB; Latronico AC; Silveira LFG Eur J Endocrinol; 2019 Aug; 181(2):103-119. PubMed ID: 31200363 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]