Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22Guo%2C+Tingwei%22&type=Person&page=5
/vufind/Search/Results?lookfor=%22Guo%2C+Tingwei%22&type=Person&page=5
Search /vufind/Search2/Results?lookfor=%22Guo%2C+Tingwei%22&type=Person&page=5
PubPharm (88)
41
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome
enthalten in:
Human genetics
| 2016
von
Mlynarski, E.
|
Xie, M.
|
Taylor, D.
| +28
Wird geladen...
42
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome
enthalten in:
Human genetics
| 2016
von
Mlynarski, E.
|
Xie, M.
|
Taylor, D.
| +28
Wird geladen...
43
Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome
enthalten in:
Human genetics
| 2016
von
Mlynarski, E.
|
Xie, M.
|
Taylor, D.
| +28
Wird geladen...
44
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome
enthalten in:
American journal of human genetics
| 2015
von
Guo, T.
|
Chung, J.
|
Wang, T.
| +7
Wird geladen...
45
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome
enthalten in:
American journal of human genetics
| 2015
von
Mlynarski, E.
|
Sheridan, M.
|
Xie, M.
| +30
Wird geladen...
46
Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome
enthalten in:
American journal of human genetics
| 2015
von
Mlynarski, E.
|
Sheridan, M.
|
Xie, M.
| +29
Wird geladen...
47
Histone Modifier Genes Alter Conotruncal Heart Phenotypes in 22q11.2 Deletion Syndrome
enthalten in:
American journal of human genetics
| 2015
von
Guo, T.
|
Chung, J.
|
Wang, T.
| +7
Wird geladen...
48
Tbx1 is required autonomously for cell survival and fate in the pharyngeal core mesoderm to form the muscles of mastication
enthalten in:
Human molecular genetics
| 2014
von
Kong, P.
|
Racedo, S.
|
Macchiarulo, S.
| +6
Wird geladen...
49
A robust method for genome-wide association meta-analysis with the application to circulating insulin-like growth factor I concentrations
enthalten in:
Genetic epidemiology
| 2014
von
Wang, T.
|
Zhou, B.
|
Guo, T.
| +5
Wird geladen...
50
A Robust Method for Genome‐Wide Association Meta‐Analysis With the Application to Circulating Insulin‐Like Growth Factor I Concentrations
enthalten in:
Genetic epidemiology
| 2014
von
Wang, T.
|
Zhou, B.
|
Guo, T.
| +5
Wird geladen...
[1]
« Vorheriger
1
2
3
4
5
6
7
8
9
Nächster »
[9]
Filter & Sortierung
Treffer pro Seite
10
20
50
Sortieren
Relevanz
Neueste zuerst
Älteste zuerst
Verfasser
Zeitschriftentitel
Bibliothek
Standort (Printmedien)
Verwandte Substanzen
Verwandte Substanzen werden ermittelt...
Verwandte Erkrankungen/Symptome
Verwandte Erkrankungen/Symptome werden ermittelt...
Verwandte Gene
Verwandte Gene werden ermittelt...
Systematic Reviews
Clinical Studies
Patente
Covid-19/SARS-CoV-2
Exclude Systematic Reviews
Exclude Clinical Studies
Exclude Patents
Medienart
88
Aufsätze
58
E-Artikel
58
E-Ressourcen
30
Gedruckte Aufsätze
Zeitschriftentitel
10
American journal of human genetics
7
Neuroscience letters
6
Diabetes
4
Biochemical and biophysical research communicat...
4
Human molecular genetics
4
Schizophrenia research
4
bioRxiv.org
4
eLife
3
American journal of medical genetics. Part A
3
BMC medical genetics
2
Annals of human biology
2
BioMed research international
2
Development (Cambridge, England)
2
Genetic epidemiology
2
Human genetics
2
Human genetics <Berlin>
2
Human mutation
2
Molecular genetics and metabolism
2
Nature communications
2
PLoS genetics
Alle anzeigen ...
weniger ...
Thema
58
Journal Article
34
Research Support, Non-U.S. Gov't
24
Research Support, N.I.H., Extramural
4
DiGeorge syndrome
4
Research Support, N.I.H., Intramural
4
T-Box Domain Proteins
4
developmental biology
4
mouse
3
Bioinformatic analysis
3
Congenital Heart Defect
3
Histones
3
LIM homeobox transcription factor 1-beta (LMX1B)
3
Mammalian Phenotype
3
Mutation
3
Nail–patella syndrome
3
Nerve Tissue Proteins
3
Normal Cardiac Anatomy
3
Rare CNVs
3
Rare Deletion
3
Sanger sequencing
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
25
2020-
47
2010-2019
16
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
71
Englisch
Haven't found what you're looking for?
Wird geladen...
