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PMID: 16912708 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't

A complex phenotype with cystic renal disease.

Kidney international ·Vol. 70 ·No. 9 ·2006-11-00 ·Pages 1656-60

Müller D, Klopocki E, Neumann LM, Mundlos S, Taupitz M, Schulze I, Ropers HH, Querfeld U, Ullmann R

Abstract

暂无摘要

MeSH Terms
Adolescent Chromosomes, Human, Pair 17 DNA/genetics Gene Deletion Hepatocyte Nuclear Factor 1-beta/genetics Humans In Situ Hybridization, Fluorescence Kidney Diseases, Cystic/genetics,pathology,physiopathology Male Nucleic Acid Hybridization/methods Phenotype
Chemicals
HNF1B protein, human Hepatocyte Nuclear Factor 1-beta DNA
Authors & Affiliations
9 authors, click to expand affiliations / ORCID
Müller D
Department of Pediatric Nephrology, Charité Campus Virchow, Berlin, Germany. [email protected]
Klopocki E
Neumann L M
Mundlos S
Taupitz M
Schulze I
Ropers H-H
Querfeld U
Ullmann R
Article Info
Journal
Kidney international
Abbr.
Kidney Int
ISSN
0085-2538
DOI
10.1038/sj.ki.5001746
Email
[email protected]
Published
2006-11-00
Epub
2006-00-16
Pages
1656-60
Language
English
Region
United States
NLM ID
0323470
Subset
IM
External Links
PubMed source DOI: 10.1038/sj.ki.5001746 View journal details
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