Language
English
German
^M
Dutch
Spanish
Title:
De novo microduplications at 1q41, 2q37.3, and 8q24.3 in patients with VATER/VACTERL association
Source:
European Journal of Human Genetics [1018-4813] Hilger, Alina yr:2013
Basic
Full text
Full text available via
Nature
Year:
Volume:
Issue:
Start Page:
Full text available via
PubMed Central
Year:
Volume:
Issue:
Start Page:
Document delivery
Request document via
Library/Bibliothek
Users interested in this article also expressed an interest in the following:
description
1.
Sanna Cherchi, S.
"Copy-number disorders are a common cause of congenital kidney malformations."
American journal of human genetics
91.6 (2012): 987-97.
description
2.
Marzuillo, P.
"Outcomes of a Cohort of Prenatally Diagnosed and Early Enrolled Patients with Congenital Solitary Functioning Kidney."
The Journal of urology
198.5 (2017): 1153-1158.
description
3.
Handrigan, Gregory R.
"Deletions in 16q24.2 are associated with autism spectrum disorder, intellectual disability and congenital renal malformation."
Journal of medical genetics
50.3 (2013): 163-173.
description
4.
Gharavi, Ali G.
"Genome-wide association study identifies susceptibility loci for IgA nephropathy."
Nature Genetics
43.4 (2011): 321-327.
description
5.
Tomlinson, Tamra W.
"Congenital cardiovascular lesions in children with trisomy 21 at the Bustamante Hospital for Children."
Cardiology in the young
20.3 (2010): 327-331.
description
6.
Atkins, R C C.
"Glomerulonephritis."
The lancet
365.9473: 1797-1806.
description
7.
Macanovic M, M.
"Glomerulonephritis."
Medicine
31.5: 36-42.
description
8.
Pusey, Charles D.
"The changing profile of acute tubulointerstitial nephritis."
Nephrology, Dialysis, Transplantation
19.1 (2004): 8-11.
description
9.
Case, R.
"Glomerulonephritis."
The New England journal of medicine
339.13 (1998): 888-99.
description
10.
Mathieson, Peter W W.
"Glomerulonephritis."
Seminars in immunopathology
29.4 (2007): 315-6.
description
11.
Harrington, M P T.
"The diagnosis of glomerular diseases: acute glomerulonephritis and the nephrotic syndrome."
Archives of internal medicine
161.1 (2000): 25-34.
description
12.
"Yield of array‐ CGH analysis in Tunisian children with autism spectrum disorder."
Molecular genetics & genomic medicine.
10.8.
description
13.
Schreuder, Michiel F.
"Life with one kidney: response to comments by Marzuillo and Polito."
Pediatric nephrology
33.4 (2018): 725-726.
description
14.
Davidovits, M.
"Outcomes of prenatally diagnosed solitary functioning kidney during early life."
Journal of perinatology : official journal of the California Perinatal Association.
37.12: 1325-1329.
description
15.
Gardner, C.
"Shadowing: pediatric heart surgery in El Salvador."
Perspectives in Biology and Medicine
(2012): 435-442.
description
16.
Ghosh, Raktim K.
"Cardiovascular outcomes of sodium-glucose cotransporter 2 inhibitors: A comprehensive review of clinical and preclinical studies."
International journal of cardiology
212 (2016): 29-36.
description
17.
Järvinen, Tiina M.
"Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population."
Rheumatology
51.1 (2012): 87-92.
description
18.
Kaur, I.
"Mutation spectrum of fork-head transcriptional factor gene (FOXL2) in Indian blepharophimosis ptosis epicanthus inversus syndrome (BPES) patients."
British journal of ophthalmology
95.6 (2011): 881-886.
description
19.
Gesualdo, Gudmar G.
"Geographic Differences in Genetic Susceptibility to IgA Nephropathy: GWAS Replication Study and Geospatial Risk Analysis."
PLOS Genetics
8.6 (2012).
description
20.
Reilly, D.
"Life and Death of a Child With Down Syndrome and a Congenital Heart Condition: Experiences of Six Couples."
Intellectual and developmental disabilities
48.6 (2010): 403-416.
View More...
View Less...
Select All
Clear All
Save Citations
Select Format
RefWorks
EndNote
ProCite
Reference Manager
Submit citation export
Advanced
Author
Other articles by this author? -- in
GeoRef
author:
Hilger, Alina
Schramm, Charlotte
Pennimpede, Tracie
Wittler, Lars
Dworschak, Gabriel C
Bartels, Enrika
Engels, Hartmut
Zink, Alexander M
Degenhardt, Franziska
Müller, Annette M
Schmiedeke, Eberhard
Grasshoff Derr, Sabine
Märzheuser, Stefanie
Hosie, Stuart
Holland Cunz, Stefan
Wijers, Charlotte H
Marcelis, Carlo L
van Rooij, Iris A
Hildebrandt, Friedhelm
Herrmann, Bernhard G
Nöthen, Markus M
Ludwig, Michael
Reutter, Heiko
Draaken, Markus
last name
initials
Other articles by this author? -- in
Online Contents Geosciences
author:
Hilger, Alina
Schramm, Charlotte
Pennimpede, Tracie
Wittler, Lars
Dworschak, Gabriel C
Bartels, Enrika
Engels, Hartmut
Zink, Alexander M
Degenhardt, Franziska
Müller, Annette M
Schmiedeke, Eberhard
Grasshoff Derr, Sabine
Märzheuser, Stefanie
Hosie, Stuart
Holland Cunz, Stefan
Wijers, Charlotte H
Marcelis, Carlo L
van Rooij, Iris A
Hildebrandt, Friedhelm
Herrmann, Bernhard G
Nöthen, Markus M
Ludwig, Michael
Reutter, Heiko
Draaken, Markus
last name
initials
Other articles by this author? -- using
Web of Science
author:
Hilger, Alina
Schramm, Charlotte
Pennimpede, Tracie
Wittler, Lars
Dworschak, Gabriel C
Bartels, Enrika
Engels, Hartmut
Zink, Alexander M
Degenhardt, Franziska
Müller, Annette M
Schmiedeke, Eberhard
Grasshoff Derr, Sabine
Märzheuser, Stefanie
Hosie, Stuart
Holland Cunz, Stefan
Wijers, Charlotte H
Marcelis, Carlo L
van Rooij, Iris A
Hildebrandt, Friedhelm
Herrmann, Bernhard G
Nöthen, Markus M
Ludwig, Michael
Reutter, Heiko
Draaken, Markus
last name
initials
Web Search
Find related information in
a Web Search Engine
Excite
Google
HotBot
Ixquick
ZOO
Ask
Yahoo!
Bing
Naver
Search Terms:
Search for related information in
Google Scholar
Article Title
Author Name
Journal Title
Other Search
Search Terms:
A service provided by the
Library of the Wissenschaftspark Albert Einstein
, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.