| scholarly article | Q13442814 |
| P50 | author | Qin Yang | Q64746728 |
| P2093 | author name string | Xu Ma | |
| Ge Gao | |||
| Guo-Wei He | |||
| Chao Xuan | |||
| Xiao-Cheng Liu | |||
| Xiao-Yan Bai | |||
| Bin-Bin Wang | |||
| Wen-Bin Jing | |||
| P2860 | cites work | Tissue-specific imprinting of the ZAC/PLAGL1 tumour suppressor gene results from variable utilization of monoallelic and biallelic promoters. | Q51992629 |
| Imprinting mechanisms in mammals. | Q52187194 | ||
| Assessing familial aggregation of congenital cardiovascular malformations in case-control studies. | Q53747309 | ||
| Transcription: Enhancers make non-coding RNA. | Q55052904 | ||
| Recurrence of Discordant Congenital Heart Defects in Families | Q63353099 | ||
| Congenital heart disease among 815,569 children born between 1980 and 1990 and their 15-year survival: a prospective Bohemia survival study | Q73169183 | ||
| Prevalence and pattern of congenital heart disease in Hazara | Q77714466 | ||
| Focal giant cell cardiomyopathy with Beckwith-Wiedemann syndrome | Q93687313 | ||
| ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome | Q24301866 | ||
| The cell cycle control gene ZAC/PLAGL1 is imprinted--a strong candidate gene for transient neonatal diabetes | Q28143868 | ||
| Congenital ventricular septal defects and prenatal exposure to cyclooxygenase inhibitors | Q28199711 | ||
| Alternative splicing of the imprinted candidate tumor suppressor gene ZAC regulates its antiproliferative and DNA binding activities | Q28213694 | ||
| Hypomethylation at multiple maternally methylated imprinted regions including PLAGL1 and GNAS loci in Beckwith-Wiedemann syndrome. | Q34326159 | ||
| Incidence and natural course of trabecular ventricular septal defect: two-dimensional echocardiography and color Doppler flow imaging study | Q34350418 | ||
| Establishment of the primary imprint of the HYMAI/PLAGL1 imprint control region during oogenesis | Q34507201 | ||
| Incidence and risk factors for ventricular septal defect in "low risk" neonates | Q35288485 | ||
| Genomic imprinting in mammals: its life cycle, molecular mechanisms and reprogramming | Q35347999 | ||
| Genetic and non-genetic factors in the etiology of congenital heart disease: a study of 1188 cases | Q35911435 | ||
| Epigenetic deregulation of imprinting in congenital diseases of aberrant growth | Q36449310 | ||
| Congenital cardiac abnormalities in monozygotic twins. Report and review of the literature | Q36769567 | ||
| Demonstration of all-or-none loss of imprinting in mRNA expression in single cells. | Q37467351 | ||
| Environmental risk factors for congenital heart disease in the Shandong Peninsula, China: a hospital-based case-control study | Q37583267 | ||
| The changing epidemiology of congenital heart disease | Q37806606 | ||
| Zac1 is an essential transcription factor for cardiac morphogenesis. | Q38346339 | ||
| Genetic analysis of cardiac-specific transcription factors reveals novel insights into molecular causes of congenital heart disease | Q38443001 | ||
| LOT1 (ZAC1/PLAGL1) as member of an imprinted gene network does not harbor Silver-Russell specific variants | Q43513058 | ||
| Congenital heart disease: prevalence at livebirth. The Baltimore-Washington Infant Study | Q46070194 | ||
| P433 | issue | 8 | |
| P921 | main subject | ventricular septal defect | Q838139 |
| P304 | page(s) | 984-987 | |
| P577 | publication date | 2012-07-11 | |
| P1433 | published in | Genetic Testing and Molecular Biomarkers | Q15753742 |
| P1476 | title | A novel variation of PLAGL1 in Chinese patients with isolated ventricular septal defect | |
| P478 | volume | 16 |
| Q41284394 | Acute phase proteins altered in the plasma of patients with congenital ventricular septal defect |
| Q34628733 | Association between MTHFR polymorphisms and congenital heart disease: a meta-analysis based on 9,329 cases and 15,076 controls |
| Q94475259 | Corrective surgery alters plasma protein profiling in congenital heart diseases and clinical perspectives |
| Q36789447 | Identification of two novel mutations of the HOMEZ gene in Chinese patients with isolated ventricular septal defect |
| Q57170707 | Meta-Prediction of MTHFR Gene Polymorphism and Air Pollution on the Risks of Congenital Heart Defects Worldwide: A Transgenerational Analysis |
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