- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
Rare variants analyses suggest novel cleft genes in the African population ; volume:14 ; number:1 ; day:20 ; month:6 ; year:2024 ; pages:1-10 ; date:12.2024
Scientific reports ; 14, Heft 1 (20.6.2024), 1-10, 12.2024
- Urheber
-
Alade, Azeez
Mossey, Peter
Awotoye, Waheed
Busch, Tamara
Oladayo, Abimbola M.
Aladenika, Emmanuel
Olujitan, Mojisola
Wentworth, Emma
Anand, Deepti
Naicker, Thirona
Gowans, Lord J. J.
Eshete, Mekonen A.
Adeyemo, Wasiu L.
Zeng, Erliang
Otterloo, Eric Van
O’Rorke, Michael
Adeyemo, Adebowale
Murray, Jeffrey C.
Cotney, Justin
Lachke, Salil A.
Romitti, Paul
Butali, Azeez
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41598-024-65151-9
- URN
-
urn:nbn:de:101:1-2409160920319.495888268193
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:25 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Alade, Azeez
- Mossey, Peter
- Awotoye, Waheed
- Busch, Tamara
- Oladayo, Abimbola M.
- Aladenika, Emmanuel
- Olujitan, Mojisola
- Wentworth, Emma
- Anand, Deepti
- Naicker, Thirona
- Gowans, Lord J. J.
- Eshete, Mekonen A.
- Adeyemo, Wasiu L.
- Zeng, Erliang
- Otterloo, Eric Van
- O’Rorke, Michael
- Adeyemo, Adebowale
- Murray, Jeffrey C.
- Cotney, Justin
- Lachke, Salil A.
- Romitti, Paul
- Butali, Azeez
- SpringerLink (Online service)
Ähnliche Objekte (12)
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
Repair of bilateral cleft lip and its variants
Repair of bilateral cleft lip and its variants
Pan-cancer analyses suggest kindlin-associated global mechanochemical alterations
Functional stability analyses of maxillofacial skeleton bearing cleft deformities
Cleft palate: a rare complication following esophageal stent implantation
Complete cleft of the upper limb: A very rare anomaly
Complete cleft of the upper limb: A very rare anomaly
Roberts-SC syndrome, a rare syndrome and cleft palate repair
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores
Functional analyses of rare germline BRCA1 variants by transcriptional activation and homologous recombination repair assays
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
Repair of bilateral cleft lip and its variants
Repair of bilateral cleft lip and its variants
Pan-cancer analyses suggest kindlin-associated global mechanochemical alterations
Functional stability analyses of maxillofacial skeleton bearing cleft deformities
Cleft palate: a rare complication following esophageal stent implantation
Complete cleft of the upper limb: A very rare anomaly
Complete cleft of the upper limb: A very rare anomaly
Roberts-SC syndrome, a rare syndrome and cleft palate repair
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores
Functional analyses of rare germline BRCA1 variants by transcriptional activation and homologous recombination repair assays
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
Repair of bilateral cleft lip and its variants
Repair of bilateral cleft lip and its variants
Pan-cancer analyses suggest kindlin-associated global mechanochemical alterations
Functional stability analyses of maxillofacial skeleton bearing cleft deformities
Cleft palate: a rare complication following esophageal stent implantation
Complete cleft of the upper limb: A very rare anomaly
Complete cleft of the upper limb: A very rare anomaly
Roberts-SC syndrome, a rare syndrome and cleft palate repair
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients
Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores