37 related articles for article (PubMed ID: 34549882)
1. A novel NONO nonsense variant in a fetus with renal abnormalities.
Rodriguez-Revenga L; Nadal A; Borobio V; Álvarez-Mora MI; Madrigal I; Pauta M; Borrell A
Prenat Diagn; 2024 Jan; 44(1):77-80. PubMed ID: 38110236
[TBL] [Abstract][Full Text] [Related]
2. X-linked intellectual developmental disorder with onset of neonatal heart failure: A case report and literature review.
Xi H; Ma L; Yin X; Yang P; Li X; Li L
Mol Genet Metab Rep; 2024 Mar; 38():101054. PubMed ID: 38469091
[TBL] [Abstract][Full Text] [Related]
3. Case Report: Non-ossifying fibromas with pathologic fractures in a patient with
Writzl K; Mavčič B; Maver A; Hodžić A; Peterlin B
Front Genet; 2023; 14():1167054. PubMed ID: 37533431
[TBL] [Abstract][Full Text] [Related]
4. Altered contractility, Ca
Thareja SK; Anfinson M; Cavanaugh M; Kim MS; Lamberton P; Radandt J; Brown R; Liang HL; Stamm K; Afzal MZ; Strande J; Frommelt MA; Lough JW; Fitts RH; Mitchell ME; Tomita-Mitchell A
Am J Physiol Heart Circ Physiol; 2023 Jul; 325(1):H149-H162. PubMed ID: 37204873
[TBL] [Abstract][Full Text] [Related]
5. Nono deficiency impedes the proliferation and adhesion of H9c2 cardiomyocytes through Pi3k/Akt signaling pathway.
Lei YQ; Ye ZJ; Wei YL; Zhu LP; Zhuang XD; Wang XR; Cao H
Sci Rep; 2023 May; 13(1):7134. PubMed ID: 37130848
[TBL] [Abstract][Full Text] [Related]
6. Undiagnosed disease program in South Africa: Results from first 100 exomes.
Moosa S; Coetzer KC; Lee E; Seo GH
Am J Med Genet A; 2022 Sep; 188(9):2684-2692. PubMed ID: 35616356
[TBL] [Abstract][Full Text] [Related]
7. A Systematic Review of Ebstein's Anomaly with Left Ventricular Noncompaction.
Thareja SK; Frommelt MA; Lincoln J; Lough JW; Mitchell ME; Tomita-Mitchell A
J Cardiovasc Dev Dis; 2022 Apr; 9(4):. PubMed ID: 35448091
[TBL] [Abstract][Full Text] [Related]
8. Genetic and phenotypic spectrum in the NONO-associated syndromic disorder.
Roessler F; Beck AE; Susie B; Tobias B; Begtrup A; Biskup S; Caluseriu O; Delanty N; Fröhlich C; Greally MT; Karnstedt M; Klöckner C; Kurtzberg J; Schubert S; Schulze M; Weidenbach M; Westphal DS; White M; Wolf CM; Zyskind J; Popp B; Strehlow V
Am J Med Genet A; 2023 Feb; 191(2):469-478. PubMed ID: 36426740
[TBL] [Abstract][Full Text] [Related]
9. Ebstein's anomaly: a complex congenital heart defect.
Cherry C; DeBord S; Moustapha-Nadler N
AORN J; 2009 Jun; 89(6):1098-110; quiz 1111-4. PubMed ID: 19606562
[TBL] [Abstract][Full Text] [Related]
10. Novel hemizygous loss-of-function variant in NONO identified in a South African boy.
Coetzer KC; Moosa S
Am J Med Genet A; 2022 Jan; 188(1):373-376. PubMed ID: 34549882
[TBL] [Abstract][Full Text] [Related]
11. Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO.
Scott DA; Hernandez-Garcia A; Azamian MS; Jordan VK; Kim BJ; Starkovich M; Zhang J; Wong LJ; Darilek SA; Breman AM; Yang Y; Lupski JR; Jiwani AK; Das B; Lalani SR; Iglesias AD; Rosenfeld JA; Xia F
J Med Genet; 2017 Jan; 54(1):47-53. PubMed ID: 27550220
[TBL] [Abstract][Full Text] [Related]
12. 3'UTR Deletion of
Giuffrida MG; Goldoni M; Genovesi ML; Carpentieri G; Torres B; Deac AD; Cecchetti S; Martinelli A; Vaisfeld A; Flex E; Bernardini L
Diagnostics (Basel); 2022 Sep; 12(10):. PubMed ID: 36292043
[No Abstract] [Full Text] [Related]
13. Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONO.
Sewani M; Nugent K; Blackburn PR; Tarnowski JM; Hernandez-Garcia A; Amiel J; Whalen S; Keren B; Courtin T; Rosenfeld JA; Yang Y; Patterson MC; Pichurin P; McLean SD; Scott DA
Am J Med Genet A; 2020 Apr; 182(4):652-658. PubMed ID: 31883306
[TBL] [Abstract][Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
