Author/Creator: Men, Meichao - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Men, Meichao

1. Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadism. Issue 11 (11th October 2021)

Authors:: Men, Meichao; Chen, Dan‐Na; Li, Jia‐Da; Wang, Xinying; Zeng, Wang; Jiang, Fang; Zheng, Ruizhi; Dai, Wenting
Journal:: Molecular genetics & genomic medicine
Issue:: Volume 9:Issue 11(2021)
Page Start:: n/a
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism. Issue 3 (September 2020)

Authors:: Hou, Qiao; Wu, Jiayu; Zhao, Yaguang; Wang, Xinying; Jiang, Fang; Chen, Dan-Na; Zheng, Ruizhi; Men, Meichao; Li, Jia-Da
Journal:: European journal of endocrinology
Issue:: Volume 183:Issue 3(2020)
Page Start:: 245
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadism. Issue 3 (September 2020)

Authors:: Hou, Qiao; Wu, Jiayu; Zhao, Yaguang; Wang, Xinying; Jiang, Fang; Chen, Dan-Na; Zheng, Ruizhi; Men, Meichao; Li, Jia-Da
Journal:: European journal of endocrinology
Issue:: Volume 183:Issue 3(2020)
Page Start:: 245
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

4. Identification of a Novel CNV at 8q13 in a Family With Branchio‐Oto‐Renal Syndrome and Epilepsy. (25th March 2019)

Authors:: Men, Meichao; Li, Wu; Chen, Hongsheng; Wu, Jiayu; Feng, Yong; Guo, Hui; Li, Jia‐Da
Journal:: Laryngoscope
Issue:: Volume 130:Number 2(2020)
Page Start:: 526
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

5. MITF Is Mutated in Type 1 Waardenburg Syndrome With Unusual Phenotype. Issue 10 (December 2020)

Authors:: Li, Wu; Feng, Yong; Chen, Hongsheng; He, Chufeng; Mei, Lingyun; Liu, Xue Zhong; Men, Meichao
Journal:: Otology & neurotology
Issue:: Volume 41:Issue 10(2020)
Page Start:
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

6. Prevalence and associated phenotypes of DUSP6, IL17RD and SPRY4 variants in a large Chinese cohort with isolated hypogonadotropic hypogonadism. Issue 1 (10th May 2020)

Authors:: Men, Meichao; Wang, Xinying; Wu, Jiayu; Zeng, Wang; Jiang, Fang; Zheng, Ruizhi; Li, Jia-Da
Journal:: Journal of medical genetics
Issue:: Volume 58:Issue 1(2021)
Page Start:: 66
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗