Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Abnormalities and IHH[original query] |
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Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism. Fertility and sterility 2014 Oct 102 (4): 1130-1136.e3. Izumi Yoko, Suzuki Erina, Kanzaki Susumu, Yatsuga Shuichi, Kinjo Saori, Igarashi Maki, Maruyama Tetsuo, Sano Shinichiro, Horikawa Reiko, Sato Naoko, Nakabayashi Kazuhiko, Hata Kenichiro, Umezawa Akihiro, Ogata Tsutomu, Yoshimura Yasunori, Fukami Ma |
Spectrum of phenotype and genotype of congenital isolated hypogonadotropic hypogonadism in Asian Indians. Clinical endocrinology 2015 Dec . Nair Sandhya, Jadhav Swati, Lila Anurag, Jagtap Varsha, Bukan Amol, Pandit Reshma, Ekbote Alka, Dharmalingam Mala, Kumar Prasanna, Kalra Pramila, Gandhi Pramod, Walia Rama, Sankhe Shilpa, Raghavan Vijaya, Shivane Vyankatesh, Menon Padma, Bandgar Tushar, Shah Nali |
[Children with idiopathic hypogonadotropic hypogonadism: clinical data analysis and mutations analysis of KAL1 and FGFR1 gene]. Zhonghua er ke za zhi. Chinese journal of pediatrics 2014 Dec 52 (12): 942-7. Qin Miao, Gong Chunxiu, Qi Zhan, Wu Di, Liu Min, Gu Yi, Cao Bingyan, Li Wenjing, Liang Xuej |
IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy. The Journal of clinical endocrinology and metabolism 2017 11 103 (2): 604-614. Vasques Gabriela A, Funari Mariana F A, Ferreira Frederico M, Aza-Carmona Miriam, Sentchordi-Montané Lucia, Barraza-García Jimena, Lerario Antonio M, Yamamoto Guilherme L, Naslavsky Michel S, Duarte Yeda A O, Bertola Debora R, Heath Karen E, Jorge Alexander A |
Phenotypic Spectrum of Idiopathic Hypogonadotropic Hypogonadism Patients With CHD7 Variants From a Large Chinese Cohort. The Journal of clinical endocrinology and metabolism 2019 11 105 (5): . Li Jia-Da, Wu Jiayu, Zhao Yaguang, Wang Xinying, Jiang Fang, Hou Qiao, Chen Dan-Na, Zheng Ruizhi, Yu Renhe, Zhou Wei, Men Meich |
Integrative analysis of genomic and epigenetic regulation of endometrial cancer. Aging 2020 5 12 (10): 9260-9274. Zhong Qihang, Fan Junpeng, Chu Honglei, Pang Mujia, Li Junsheng, Fan Yong, Liu Ping, Wu Congying, Qiao Jie, Li Rong, Hang Ji |
The p190 RhoGAPs, ARHGAP35, and ARHGAP5 are implicated in GnRH neuronal development: Evidence from patients with idiopathic hypogonadotropic hypogonadism, zebrafish, and in vitro GAP activity assay. Genetics in medicine : official journal of the American College of Medical Genetics 2022 Sep . Lippincott Margaret F, Xu Wanxue, Smith Abigail A, Miao Xinyu, Lafont Agathe, Shennib Omar, Farley Gordon J, Sabbagh Riwa, Delaney Angela, Stamou Maria, Plummer Lacey, Salnikov Kathryn, Georgopoulos Neoklis A, Mericq Veronica, Quinton Richard, Mau-Them Frederic Tran, Nambot Sophie, Hamad Asma, Brittain Helen, Tooze Rebecca S, Calpena Eduardo, Wilkie Andrew O M, Willems Marjolaine, Crowley William F, Balasubramanian Ravikumar, Lamarche-Vane Nathalie, Davis Erica E, Seminara Stephanie |
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- Page last updated:Apr 16, 2024
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