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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2005 | 1 |
2019 | 1 |
2021 | 1 |
2022 | 2 |
2024 | 0 |
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Page 1
Splicing in action: assessing disease causing sequence changes.
J Med Genet. 2005 Oct;42(10):737-48. doi: 10.1136/jmg.2004.029538.
J Med Genet. 2005.
PMID: 16199547
Free PMC article.
Review.
Targeted panel sequencing in pediatric primary cardiomyopathy supports a critical role of TNNI3.
Kühnisch J, Herbst C, Al-Wakeel-Marquard N, Dartsch J, Holtgrewe M, Baban A, Mearini G, Hardt J, Kolokotronis K, Gerull B, Carrier L, Beule D, Schubert S, Messroghli D, Degener F, Berger F, Klaassen S.
Kühnisch J, et al.
Clin Genet. 2019 Dec;96(6):549-559. doi: 10.1111/cge.13645. Epub 2019 Oct 22.
Clin Genet. 2019.
PMID: 31568572
Item in Clipboard
Molecular analysis of dilated and left ventricular noncompaction cardiomyopathies in Egyptian children.
Mehaney DA, Haghighi A, Embaby AK, Zeyada RA, Darwish RK, Elfeel NS, Abouelhoda M, El-Saiedi SA, Gohar NA, Seliem ZS.
Mehaney DA, et al.
Cardiol Young. 2022 Feb;32(2):295-300. doi: 10.1017/S1047951121002055. Epub 2021 May 26.
Cardiol Young. 2022.
PMID: 34036930
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Molecular Diagnosis of Primary Cardiomyopathy in 231 Unrelated Pediatric Cases by Panel-Based Next-Generation Sequencing: A Major Focus on Five Carriers of Biallelic TNNI3 Pathogenic Variants.
Janin A, Perouse de Montclos T, Nguyen K, Consolino E, Nadeau G, Rey G, Bouchot O, Blanchet P, Sabbagh Q, Cazeneuve C, El-Malti R, Morel E, Delinière A, Chevalier P, Millat G.
Janin A, et al.
Mol Diagn Ther. 2022 Sep;26(5):551-560. doi: 10.1007/s40291-022-00604-3. Epub 2022 Jul 15.
Mol Diagn Ther. 2022.
PMID: 35838873
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