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=%22Megarbane%2C+Andre%22&type=Person&page=8
/vufind/Search/Results?lookfor=%22Megarbane%2C+Andre%22&type=Person&page=8
Search /vufind/Search2/Results?lookfor=%22Megarbane%2C+Andre%22&type=Person&page=8
PubPharm (489)
71
Transcriptomic study in women with trisomy 21 identifies a possible role of the GTPases of the immunity-associated proteins (GIMAP) in the protection of breast cancer
enthalten in:
Scientific reports
| 2020
von
Mégarbané, A.
|
Piquemal, D.
|
Rebillat, A.
| +9
Wird geladen...
72
Homozygous deletion of exons 2-7 within TGFB3 gene in a child with severe Loeys-Dietz syndrome and Marfan-like features
enthalten in:
American journal of medical genetics. Part A
| 2020
von
Mégarbané, A.
|
Deepthi, A.
|
Obeid, M.
| +3
Wird geladen...
73
Recessive marfanoid syndrome with herniation associated with a homozygous mutation in Fibulin-3
enthalten in:
European journal of medical genetics
| 2020
von
Bizzari, S.
|
El-Bazzal, L.
|
Nair, P.
| +6
Wird geladen...
74
Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster
enthalten in:
European journal of human genetics : EJHG
| 2020
von
Le Caignec, C.
|
Pichon, O.
|
Briand, A.
| +13
Wird geladen...
75
Turner syndrome in diverse populations
enthalten in:
American journal of medical genetics. Part A
| 2020
von
Kruszka, P.
|
Addissie, Y.
|
Tekendo-Ngongang, C.
| +49
Wird geladen...
76
CNTNAP1 Mutations and Their Clinical Presentations : New Case Report and Systematic Review
enthalten in:
Case reports in medicine
| 2020
von
Sabbagh, S.
|
Antoun, S.
|
Mégarbané, A.
Wird geladen...
77
A Report on a Family with TMTC3-Related Syndrome and Review
enthalten in:
Case reports in medicine
| 2020
von
Hana, S.
|
Karthik, D.
|
Shan, J.
| +3
Wird geladen...
78
Turner syndrome in diverse populations
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2020
von
Kruszka, P.
|
Addissie, Y.
|
Tekendo‐Ngongang, C.
| +49
Wird geladen...
79
Homozygous deletion of exons 2–7 within TGFB3 gene in a child with severe Loeys‐Dietz syndrome and Marfan‐like features
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2020
von
Mégarbané, A.
|
Deepthi, A.
|
Obeid, M.
| +3
Wird geladen...
80
Developmental delay, intellectual disability, short stature, subglottic stenosis, hearing impairment, onychodysplasia of the index fingers, and distinctive facial features : A newly reported autosomal recessive syndrome
enthalten in:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics
| 2020
von
Mégarbané, A.
|
Hana, S.
|
El‐Hayek, S.
| +3
Wird geladen...
[1]
« Vorheriger
3
4
5
6
7
8
9
10
11
12
13
Nächster »
[49]
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
489
Aufsätze
290
E-Artikel
290
E-Ressourcen
199
Gedruckte Aufsätze
Zeitschriftentitel
43
American journal of medical genetics. Part A
32
American journal of human genetics
26
European journal of medical genetics
21
American journal of medical genetics / C
16
American journal of medical genetics
14
European journal of human genetics : EJHG
14
Human mutation
12
BMC medical genetics
12
Human genetics
11
Human genetics <Berlin>
11
Nature genetics
10
Neurogenetics
8
Human molecular genetics
8
Journal of medical genetics
8
Orphanet journal of rare diseases
7
Ophthalmic genetics
6
BMC genetics
6
BMC medical genomics
6
Brain
6
Brain : a journal of neurology
Alle anzeigen ...
weniger ...
Thema
251
Journal Article
157
Research Support, Non-U.S. Gov't
91
Case Reports
20
Research Support, N.I.H., Extramural
19
Review
17
Lebanon
13
Mutation
13
Proteins
12
Extracellular Matrix Proteins
12
Membrane Proteins
10
DNA
10
Pyrin
9
9007-49-2
8
Codon, Nonsense
8
Cytoskeletal Proteins
8
EC 2.7.11.1
8
Exome
8
Genetic Markers
8
MEFV protein, human
8
Transcription Factors
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
74
2020-
237
2010-2019
131
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
362
Englisch
6
Französisch
Haven't found what you're looking for?
Wird geladen...