Suchergebnisse - "Liu, Yalan"

PubPharm (6)

1

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

enthalten in: Human genetics | 2018

von Wang, L. | Feng, Y. | Yan, D. | +10

2

A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss

enthalten in: Human genetics | 2018

von Wang, L. | Feng, Y. | Yan, D. | +10

3

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

enthalten in: Human genetics | 2018

von Li, W. | Sun, J. | Ling, J. | +19

4

ELMOD3, a novel causative gene, associated with human autosomal dominant nonsyndromic and progressive hearing loss

enthalten in: Human genetics | 2018

von Li, W. | Sun, J. | Ling, J. | +19

5

Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population

enthalten in: Human genetics | 2012

von Hu, Z. | Xiong, Z. | Xu, X. | +15

6

Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population

enthalten in: Human genetics | 2012

von Hu, Z. | Xiong, Z. | Xu, X. | +15

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