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Frontiers in Pediatrics|April 25, 2020
The First COL4A5 Exon 41A Glycine Substitution in a Family With Alport SyndromeFang Wang, Dan Zhao, Jie Ding, et al.
Zhonghua Yi Xue Za Zhi|January 8, 2013
[Application of multiplex ligation-dependent probe amplification in gene diagnosis of X-linked Alport syndrome]Yan-qin Zhang, Dan Zhao, Li-xia Yu, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|October 29, 2009
The first Chinese Pierson syndrome with novel mutations in LAMB2Dan Zhao, Jie Ding, Fang Wang, et al.
Pediatric Nephrology (Berlin, Germany)|August 19, 2007
WT1 mutation and podocyte molecular expression in a Chinese Frasier syndrome patientJianguo Li, Dan Zhao, Jie Ding, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|January 10, 2008
Clinical characteristics and WT1 genetic analysis of patients with steroid resistant nephrotic syndrome accompanied with genitourinary malformationsJian-guo Li, Dan Zhao, Jie Ding, et al.
American Journal of Medical Genetics. Part A|August 14, 2012
Genotype-phenotype correlations in 17 Chinese patients with autosomal recessive Alport syndromeYanqin Zhang, Fang Wang, Jie Ding, et al.
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