Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Abnormalities and Nkx2-5[original query] |
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Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. Journal of the American College of Cardiology 2003 Jun 41 (11): 2072-6. Elliott David A, Kirk Edwin P, Yeoh Thomas, Chandar Suchitra, McKenzie Fiona, Taylor Peter, Grossfeld Paul, Fatkin Diane, Jones Owen, Hayes Peter, Feneley Michael, Harvey Richard |
GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease. Chinese medical journal 2009 Feb 122 (4): 4. Zhang WM, Li XF, Ma ZY, Zhang J, Zhou SH, Li T, Shi L, Li ZZ |
R25C mutation in the NKX2.5 gene in Italian patients affected with non-syndromic and syndromic congenital heart disease. Journal of cardiovascular medicine (Hagerstown, Md.) 2013 Aug 14 (8): 582-6. Beffagna Giorgia, Cecchetto Antonella, Dal Bianco Lucia, Lorenzon Alessandra, Angelini Annalisa, Padalino Massimo, Vida Vladimiro, Bhattacharya Shoumo, Stellin Giovanni, Rampazzo Alessandra, Daliento Lucia |
Linking genomic lesions with minimal residual disease improves prognostic stratification in children with T-cell acute lymphoblastic leukaemia. Leukemia research 2013 Aug 37 (8): 928-35. La Starza Roberta, Lettieri Antonella, Pierini Valentina, Nofrini Valeria, Gorello Paolo, Songia Simona, Crescenzi Barbara, Te Kronnie Geertruy, Giordan Marco, Leszl Anna, Valsecchi Maria Grazia, Aversa Franco, Basso Giuseppe, Biondi Andrea, Conter Valentino, Cazzaniga Giovanni, Mecucci Cristi |
Analysis of NKX2-5 in 439 Chinese Patients with Sporadic Atrial Septal Defect. Medical science monitor : international medical journal of experimental and clinical research 2019 Apr 25 2756-2763. Wang Hongshu, Liu Yong, Li Yaxiong, Wang Wenju, Li Lin, Meng Mingyao, Xie Yanhua, Zhang Yayong, Yunfeng Zi, Han Shen, Zeng Jianying, Hou ZongLiu, Jiang Liho |
Is Benign Hereditary Chorea Really Benign? Brain-Lung-Thyroid Syndrome Caused by NKX2-1 Mutations. Movement disorders clinical practice 2019 2 6 (1): 34-39. Parnes Mered, Bashir Hassaan, Jankovic Jose |
Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of clinical endocrinology and metabolism 2021 Mar . Vishnopolska Sebastian Alexis, Mercogliano Maria Florencia, Camilletti Maria Andrea, Mortensen Amanda Helen, Braslavsky Debora, Keselman Ana, Bergadá Ignacio, Olivieri Federico, Miranda Lucas, Marino Roxana, Ramírez Pablo, Pérez Garrido Natalia, Patiño Mejia Helen, Ciaccio Marta, Di Palma Maria Isabel, Belgorosky Alicia, Martí Marcelo Adrian, Kitzman Jacob Otto, Camper Sally Ann, Pérez-Millán Maria In |
A Case-Control Study of the Relationship Between Genetic Polymorphism and Cretinism in Xinjiang. Pharmacogenomics and personalized medicine 2023 8 16 785-794. Jia Huang, Haiyan Wu, Guiqiang Zhao, Yan Ma, Yunping An, Li Sun, Fuye Li, Shengling Wa |
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- Page last updated:Apr 16, 2024
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