E-LIB Suche - Ergebnisse für: Habulieti, Xiaerbati

1

Panoramic variation analysis of a family with neurodevelopm..:

Sun, Liwei ; Yang, Xueting ; Khan, Amjad...
Frontiers of Medicine. 18 (2023) 1 - p. 81-97 , 2023

Link: https://doi.org/10.1007/..

2

A compound heterozygous Chinese patient with xeroderma pigm..:

Habulieti, Xiaerbati ; Guo, Kexin ; Liu, Jiawei...
Experimental Dermatology. 32 (2022) 4 - p. 564-566 , 2022

Link: https://doi.org/10.1111/..

3

Novel variants in LAMA3 and COL7A1 and recurrent variant in..:

Wang, Rongrong ; Sun, Liwei ; Habulieti, Xiaerbati...
Frontiers of Medicine. 16 (2022) 5 - p. 808-814 , 2022

Link: https://doi.org/10.1007/..

4

Two novel SASH1 mutations in Chinese families with dyschrom..:

Liu, Jia‐Wei ; Habulieti, Xiaerbati ; Wang, Rong‐rong..
Journal of Clinical Laboratory Analysis. 35 (2021) 6 - p. , 2021

Link: https://doi.org/10.1002/..

5

Identification and Splicing Characterization of Novel TMC6 ..:

Wang, Rongrong ; Liu, Jiawei ; Yang, Xueting...
Frontiers in Genetics. 12 (2021) - p. , 2021

Link: https://doi.org/10.3389/..

6

Zwei neue Genmutationen verursachen unterschiedliche Ausprä..:

Habulieti, Xiaerbati ; Wang, Rongrong ; Liu, Jiawei..
JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 19 (2021) 2 - p. 271-273 , 2021

Link: https://doi.org/10.1111/..

7

Phenotypic and genetic characterization of novel variant in..:

Habulieti, Xiaerbati ; Sun, Liwei ; Liu, Jiawei...
Science China Life Sciences. 64 (2021) 12 - p. 2206-2209 , 2021

Link: https://doi.org/10.1007/..

8

Two novel gene mutations cause different expressions of epi..:

Habulieti, Xiaerbati ; Wang, Rongrong ; Liu, Jiawei..
JDDG: Journal der Deutschen Dermatologischen Gesellschaft. 19 (2020) 2 - p. 272-274 , 2020

Link: https://doi.org/10.1111/..

9

Phenotypic Characterization of Intellectual Disability Caus..:

Sun, Liwei ; Khan, Amjad ; Zhang, Han...
Frontiers in Pediatrics. 8 (2020) - p. , 2020

Link: https://doi.org/10.3389/..

10

Novel Compound Heterozygous Mutations in TTI2 Cause Syndrom..:

Wang, Rongrong ; Han, Shirui ; Liu, Hongyan...
Frontiers in Genetics. 10 (2019) - p. , 2019

Link: https://doi.org/10.3389/..

11

An unusual case of tertiary syphilis:

Ha-bu-lie-ti, Xia-er-ba-ti ; Wang, Ling-ling ; Zhu, Ya-lin
Clinical and Experimental Dermatology. 47 (2022) 4 - p. 785-787 , 2022

Link: https://doi.org/10.1111/..

12

Two novel SASH1 mutations in Chinese families with dyschrom..:

Liu, Jia‐Wei ; Habulieti, Xiaerbati ; Wang, Rong‐rong..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183922/. , 2021

Link: http://www.ncbi.nlm.nih...

13

Identification and Splicing Characterization of Novel TMC6 ..:

Wang, Rongrong ; Liu, Jiawei ; Yang, Xueting...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8353250/. , 2021

Link: http://www.ncbi.nlm.nih...

14

Phenotypic Characterization of Intellectual Disability Caus..:

Sun, Liwei ; Khan, Amjad ; Zhang, Han...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7736038/. , 2020

Link: http://www.ncbi.nlm.nih...

15

A novel DLL4 missense mutation in a Chinese patient with Ad..:

Yu, Xue ; Wang, Rong-Rong ; Han, Shi-Rui...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759108/. , 2019

Link: http://www.ncbi.nlm.nih...