Phäno- und Genotypisierung von Kindern und Jugendlichen mit Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
- Alternative title
-
Pheno- and Genotyping of Children and Adolescents with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT)
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Deutsch
- Notes
-
Berlin, Medizinische Fakultät Charité - Universitätsmedizin Berlin, Dissertation, 2021
- Keyword
-
Niere
Kind
Niereninsuffizienz
- Event
-
Veröffentlichung
- (where)
-
Berlin
- (who)
-
Medizinische Fakultät Charité - Universitätsmedizin Berlin
- (when)
-
2021
- Creator
- DOI
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10.17169/refubium-29399
- URN
-
urn:nbn:de:kobv:188-refubium-29655-0
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:50 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Isert, Saskia
- Medizinische Fakultät Charité - Universitätsmedizin Berlin
Time of origin
- 2021
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Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Urinary tract
Urinary tract cytology
Urinary tract infections
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems
Rare variants in BNC2 are implicated in autosomal-dominant congenital lower urinary-tract obstruction
Congenital hand anomalies and associated syndromes
Studies on congenital anomalies in cattle
Urinary tract infections : 34 tables
The many faces of congenital anomalies of the kidney and urinary tract
Lower urinary tract dysfunction in children with congenital anomalies of the pelvic region and perineum
Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)
Urinary tract
Urinary tract cytology
Urinary tract infections
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems
X-linked variations in SHROOM4 are implicated in congenital anomalies of the urinary tract and the anorectal, cardiovascular and central nervous systems
Rare variants in BNC2 are implicated in autosomal-dominant congenital lower urinary-tract obstruction
Congenital hand anomalies and associated syndromes
Studies on congenital anomalies in cattle