| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/GENE.1074 |
| P698 | PubMed publication ID | 11536434 |
| P2093 | author name string | C J Epstein | |
| E J Carlson | |||
| P C Ursell | |||
| A M Gillespie | |||
| A J Villar | |||
| P2860 | cites work | Cardiac defects and altered ryanodine receptor function in mice lacking FKBP12 | Q28594463 |
| The mouse Gtl2 gene is differentially expressed during embryonic development, encodes multiple alternatively spliced transcripts, and may act as an RNA | Q28594499 | ||
| Genomic imprinting: implications for human disease | Q33541538 | ||
| Developmental patterning of the myocardium | Q33875810 | ||
| Identification of an imprinted gene, Meg3/Gtl2 and its human homologue MEG3, first mapped on mouse distal chromosome 12 and human chromosome 14q. | Q33897694 | ||
| Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion | Q34010175 | ||
| Genetics of heart development. | Q34023288 | ||
| Parental imprinting and human disease | Q34412350 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Roles for genomic imprinting and the zygotic genome in placental development. | Q35267816 | ||
| The imprinted gene and parent-of-origin effect database | Q38661383 | ||
| Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult | Q40969064 | ||
| Paternal uniparental disomy for chromosome 14: a case report and review | Q41454160 | ||
| Systematic approach to the study of trisomy in the mouse. II | Q41532384 | ||
| The murine situs inversus viscerum (iv) gene responsible for visceral asymmetry is linked tightly to the Igh-C cluster on chromosome 12. | Q45859032 | ||
| Delta-like and gtl2 are reciprocally expressed, differentially methylated linked imprinted genes on mouse chromosome 12. | Q52165136 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Persisting zones of slow impulse conduction in developing chicken hearts | Q68202695 | ||
| The origin of the epicardium and the embryonic myocardial circulation in the mouse | Q70993615 | ||
| Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11) | Q71788829 | ||
| Spongy myocardium | Q73938386 | ||
| Evolutionary persistence of spongy myocardium in humans | Q77726102 | ||
| P433 | issue | 4 | |
| P304 | page(s) | 274-279 | |
| P577 | publication date | 2001-08-01 | |
| P1433 | published in | Genesis | Q5532784 |
| P1476 | title | Cardiomyopathy in mice with paternal uniparental disomy for chromosome 12 | |
| P478 | volume | 30 |
| Q51947093 | Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12). | cites work | P2860 |
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