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=%22Ansar%2C+Muhammad%22&type=Person&sort=year
/vufind/Search/Results?lookfor=%22Ansar%2C+Muhammad%22&type=Person&sort=year
Search /vufind/Search2/Results?lookfor=%22Ansar%2C+Muhammad%22&type=Person&sort=year
PubPharm (266)
1
Daily Salt Intake, its Discretionary Use and Validation of Methods for Estimation using Spot Urine – Findings from Islamabad, Pakistan
enthalten in:
bioRxiv.org
| 2024
von
Nadeem Saqib, M.
|
Rafique, I.
|
Ansar, M.
| +1
Wird geladen...
2
Performance evaluation of gravity-driven bioreactor (GDB) for simultaneous treatment of black liquor and domestic wastewater
enthalten in:
Environmental science and pollution research international
| 2024
von
Rasool, T.
|
Ansar, M.
|
Ali, I.
| +5
Wird geladen...
3
A loss of function variant in AGPAT3 underlies intellectual disability and retinitis pigmentosa (IDRP) syndrome
enthalten in:
European journal of human genetics : EJHG
| 2023
von
Malik, M.
|
Saqib, M.
|
Mientjes, E.
| +9
Wird geladen...
4
Overlapping neurological phenotypes in two extended consanguineous families with novel variants in the CNTNAP1 and ADGRG1 genes
enthalten in:
The journal of gene medicine
| 2023
von
Khan, S.
|
Umair, M.
|
Abbas, S.
| +8
Wird geladen...
5
Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient
enthalten in:
Molecular biology reports
| 2023
von
Siddiqi, S.
|
Ain, N.
|
Kauser, M.
| +3
Wird geladen...
6
Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorder
enthalten in:
Genetics in medicine : official journal of the American College of Medical Genetics
| 2023
von
Mattioli, F.
|
Worpenberg, L.
|
Li, C.
| +15
Wird geladen...
7
Characterization of Vps13b-mutant mice reveals neuroanatomical and behavioral phenotypes with females less affected
enthalten in:
Neurobiology of disease
| 2023
von
Montillot, C.
|
Skutunova, E.
|
Ayushma
| +15
Wird geladen...
8
Combined Single Gene Testing and Genome Sequencing as an Effective Diagnostic Approach for Anophthalmia and Microphthalmia Patients
enthalten in:
Genes
| 2023
von
Basharat, R.
|
Rodenburg, K.
|
Rodríguez-Hidalgo, M.
| +8
Wird geladen...
9
Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient
enthalten in:
Molecular biology reports
| 2023
von
Siddiqi, S.
|
Ain, N.
|
Kauser, M.
| +3
Wird geladen...
10
Variants in FREM1 and trisomy 18 identified in a neonatal progeria patient
enthalten in:
Molecular biology reports
| 2023
von
Siddiqi, S.
|
Ain, N.
|
Kauser, M.
| +3
Wird geladen...
1
2
3
4
5
6
7
8
9
10
11
Nächster »
[27]
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
266
Aufsätze
199
E-Artikel
199
E-Ressourcen
67
Gedruckte Aufsätze
Zeitschriftentitel
25
American journal of human genetics
16
Human genetics
16
Human genetics <Berlin>
12
BMC medical genetics
10
Archives of dermatological research
10
Human molecular genetics
9
Virology journal
7
European journal of human genetics : EJHG
7
Genes
7
Molecular biology reports
7
bioRxiv.org
6
Journal of human genetics
5
Journal of dermatological science
4
International journal of dermatology
4
Japanese journal of ophthalmology
4
Journal of medical genetics
4
Nature genetics
3
American journal of medical genetics. Part A
3
BMC neurology
3
Genetics in medicine : official journal of the ...
Alle anzeigen ...
weniger ...
Thema
130
Journal Article
104
Research Support, Non-U.S. Gov't
38
Research Support, N.I.H., Extramural
14
Case Reports
10
Codon, Nonsense
9
Autosomal recessive
9
Genetic Markers
9
Membrane Proteins
8
Autosomal Recessive Mode
8
Pakistan
8
Pakistani Family
7
Nerve Tissue Proteins
7
Research Support, U.S. Gov't, P.H.S.
6
Autosomal Recessive
6
Hearing Impairment
6
Letter
6
Multipoint Linkage Analysis
5
Cell Cycle Proteins
5
Consanguinity
5
MCPH
Alle anzeigen ...
weniger ...
Erscheinungszeitraum
60
2020-
162
2010-2019
42
2000-2009
Erscheinungsjahr(e)
Von:
Bis:
Sprache
234
Englisch
Haven't found what you're looking for?
Wird geladen...