Suchergebnisse - "Wang, Pengyun"

PubPharm (4)

1

A novel FBN2 mutation cosegregates with congenital contractural arachnodactyly in a five-generation Chinese family

enthalten in: Clinical case reports | 2018

von Zhou, S. | Wang, F. | Dou, Y. | +6

2

Exomic and Epigenomic Analyses in a Pair of Monozygotic Twins Discordant for Cryptorchidism

enthalten in: Twin research and human genetics : the official journal of the International Society for Twin Studies | 2017

von Lu, P. | Wang, P. | Li, L. | +6

3

Identification of a genetic locus for autosomal dominant disseminated superficial actinic porokeratosis on chromosome 1p31.3-p31.1

enthalten in: Human genetics | 2008

von Liu, P. | Zhang, S. | Yao, Q. | +9

4

Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family

enthalten in: BMC medical genetics | 2008

von Zhang, S. | Yin, K. | Ren, X. | +7

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