Weiter zum Inhalt
Toggle navigation
English
English
Favoritenliste (
0
)
(Voll)
Kontakt
Mein Konto
Abmeldung
Mein Konto
Suche
Filter bei nächster Suche beibehalten
publishDate:"[2000 TO 2099]"
Erweiterte Suche
Suchverlauf
Struktursuche
Narrative Service
Drug Overviews
Info Guide
/vufind/Search/Results?lookfor=%22Scott%2C+Daryl+A%22&type=Person&filter%5B%5D=publishDate%3A%22%5B2000+TO+2099%5D%22
/vufind/Search/Results?lookfor=%22Scott%2C+Daryl+A%22&type=Person&filter%5B%5D=publishDate%3A%22%5B2000+TO+2099%5D%22
Search /vufind/Search2/Results?lookfor=%22Scott%2C+Daryl+A%22&type=Person&filter%5B%5D=publishDate%3A%22%5B2000+TO+2099%5D%22
PubPharm (210)
1
Exome sequencing implicates ancestry-related Mendelian variation at SYNE1 in childhood-onset essential hypertension
enthalten in:
JCI insight
| 2024
von
Copeland, I.
|
Wonkam-Tingang, E.
|
Gupta-Malhotra, M.
| +21
Wird geladen...
2
SOX7 deficiency causes ventricular septal defects through its effects on endocardial-to-mesenchymal transition and the expression of
Wnt4
and
Bmp2
enthalten in:
bioRxiv.org
| 2024
von
Hernández-García, A.
|
Kim, S.
|
Li, Y.
| +7
Wird geladen...
3
Missense variants affecting the actin-binding domains of
PLS3
cause X-linked congenital diaphragmatic hernia and body wall defects
enthalten in:
bioRxiv.org
| 2024
von
Petit, F.
|
Longoni, M.
|
Wells, J.
| +35
Wird geladen...
4
High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and Coloboma
enthalten in:
Investigative ophthalmology & visual science
| 2024
von
Kunisetty, B.
|
Martin-Giacalone, B.
|
Zhao, X.
| +8
Wird geladen...
5
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia
enthalten in:
Journal of pediatric genetics
| 2024
von
Pendleton, K.
|
Hernandez-Garcia, A.
|
Lyu, J.
| +7
Wird geladen...
6
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss-of-function variants
enthalten in:
American journal of medical genetics. Part A
| 2024
von
Sewani, S.
|
Azamian, M.
|
Mendelsohn, B.
| +20
Wird geladen...
7
Neurodevelopmental and other phenotypes recurrently associated with heterozygous BAZ2B loss‐of‐function variants
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2024
von
Sewani, S.
|
Azamian, M.
|
Mendelsohn, B.
| +20
Wird geladen...
8
Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return
enthalten in:
European journal of human genetics : EJHG
| 2023
von
Huth, E.
|
Zhao, X.
|
Owen, N.
| +29
Wird geladen...
9
Dominant negative variants in IKZF2 cause ICHAD syndrome, a new disorder characterised by immunodysregulation, craniofacial anomalies, hearing impairment, athelia and developmental delay
enthalten in:
Journal of medical genetics
| 2023
von
Mohajeri, A.
|
Vaseghi-Shanjani, M.
|
Rosenfeld, J.
| +126
Wird geladen...
10
Sox7-positive endothelial progenitors establish coronary arteries and govern ventricular compaction
enthalten in:
EMBO reports
| 2023
von
Chiang, I.
|
Humphrey, D.
|
Mills, R.
| +18
Wird geladen...
1
2
3
4
5
6
7
8
9
10
11
Nächster »
[21]
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
Ihre gewählten Filter
Filter bei nächster Suche beibehalten
Filter aufheben
Erscheinungsjahr: 2000-2099
Medienart
210
Aufsätze
150
E-Artikel
150
E-Ressourcen
60
Gedruckte Aufsätze
Zeitschriftentitel
39
Human molecular genetics
29
American journal of medical genetics. Part A
15
American journal of human genetics
15
Genetics in medicine : official journal of the ...
12
American Journal of Medical Genetics Part C: Se...
12
Journal of medical genetics
9
Human mutation
6
Genome medicine
5
PloS one
4
American journal of medical genetics / C
4
European journal of human genetics : EJHG
4
Human genetics
4
Human genetics <Berlin>
3
Journal of pediatric genetics
3
bioRxiv.org
2
American journal of medical genetics
2
Development (Cambridge, England)
2
Development <Cambridge>
2
Genome research
2
Journal of pediatric urology
Alle anzeigen ...
weniger ...
Thema
114
Journal Article
72
Research Support, N.I.H., Extramural
59
Research Support, Non-U.S. Gov't
36
Case Reports
12
DNA-Binding Proteins
10
Repressor Proteins
10
Transcription Factors
9
congenital diaphragmatic hernia
9
developmental delay
9
intellectual disability
8
Nuclear Proteins
8
Review
7
Nerve Tissue Proteins
6
EC 3.6.1.-
6
Published Erratum
5
Chromosomal Proteins, Non-Histone
5
Neurodevelopmental disorders
5
SOXF Transcription Factors
5
atrophin 2, mouse
5
autism spectrum disorder
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
2000-
81
2020-
83
2010-2019
46
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
149
Englisch
Haven't found what you're looking for?
Wird geladen...