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Journal Article
Kohl, Stefan, Chen, Jing, Vivante, Asaf, Hwang, Daw-Yang, Shril, Shirlee, Dworschak, Gabriel C., Van der Ven, Amelie, Sanna-Cherchi, Simone, Bauer, Stuart B., Lee, Richard S., Soliman, Neveen A., Kehinde, Elijah O., Reutter, Heiko M., Tasic, Velibor 
ORCID: 0000-0002-3377-1245 and Hildebrandt, Friedhelm
(2016).
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tract.
Nephrol. Dial. Transplant., 31 (8).
S. 1280 - 1284.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2385
Vivante, Asaf, Hwang, Daw-Yang, Kohl, Stefan, Chen, Jing, Shril, Shirlee, Schulz, Julian, van der Ven, Annelle, Daouk, Ghaleb, Soliman, Neveen A., Kumar, Aravind Selvin, Senguttuvan, Prabha, Kehinde, Elijah O., Tasic, Velibor ORCID: 0000-0002-3377-1245 and Hildebrandt, Friedhelm
(2017).
Exome Sequencing Discerns Syndromes in Patients from Consanguineous Families with Congenital Anomalies of the Kidneys and Urinary Tract.
J. Am. Soc. Nephrol., 28 (1).
S. 69 - 76.
WASHINGTON:
AMER SOC NEPHROLOGY.
ISSN 1533-3450
Yu, Chih-Chuan, Lee, An-Fu, Kohl, Stefen, Lin, Ming-Yen, Cheng, Siao Muk, Hung, Chi-Chih, Chang, Jer-Ming, Chiu, Yi-Wen, Hwang, Shang-Jyh, Otto, Edgar A., Hildebrandt, Friedhelm and Hwang, Daw-Yang (2022). PKD2 founder mutation is the most common mutation of polycystic kidney disease in Taiwan. npj Genom. Med., 7 (1). BERLIN: NATURE PORTFOLIO. ISSN 2056-7944
Yu, Pei-Hua, Kuo, Yuh-Ren, Altmueller, Janine and Hwang, Daw-Yang (2018). Senior-Loken syndrome with IQCB1 mutation in Taiwan. Kaohsiung J. Med. Sci., 34 (10). S. 588 - 590. TAIPEI: ELSEVIER TAIWAN. ISSN 1607-551X
van der Ven, Amelie T., Kobbe, Birgit, Kohl, Stefan, Shril, Shirlee, Pogoda, Hans-Martin, Imhof, Thomas, Ityel, Hadas, Vivante, Asaf, Chen, Jing, Hwang, Daw-Yang, Connaughton, Dervla M., Mann, Nina, Widmeier, Eugen ORCID: 0000-0002-7773-5190, Taglienti, Mary, Schmidt, Johanna Magdalena, Nakayama, Makiko, Senguttuvan, Prabha, Kumar, Selvin, Tasic, Velibor ORCID: 0000-0002-3377-1245, Kehinde, Elijah O., Mane, Shrikant M., Lifton, Richard P., Soliman, Neveen ORCID: 0000-0002-8942-1973, Lu, Weining ORCID: 0000-0002-6570-3044, Bauer, Stuart B., Hammerschmidt, Matthias, Wagener, Raimund and Hildebrandt, Friedhelm
(2018).
A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral refluxy.
PLoS One, 13 (1).
SAN FRANCISCO:
PUBLIC LIBRARY SCIENCE.
ISSN 1932-6203