| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/(SICI)1096-8628(19970502)70:1<95::AID-AJMG17>3.0.CO;2-S |
| P698 | PubMed publication ID | 9129748 |
| P2093 | author name string | Engel E | |
| P2860 | cites work | The product of the H19 gene may function as an RNA | Q24599284 |
| Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis | Q28272055 | ||
| Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient | Q28292519 | ||
| Requirement for Xist in X chromosome inactivation | Q29614509 | ||
| Sex dependent transmission of Beckwith-Wiedemann syndrome associated with a reciprocal translocation t(9;11)(p11.2;p15.5). | Q33596012 | ||
| Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15. | Q34314269 | ||
| Identification of a novel paternally expressed gene in the Prader-Willi syndrome region | Q34318139 | ||
| Uniparental paternal disomy in a genetic cancer-predisposing syndrome | Q34535432 | ||
| Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. | Q34680586 | ||
| Deletions of chromosome 15 as a cause of the Prader-Willi syndrome | Q34718526 | ||
| A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene. | Q36762586 | ||
| Genomic imprinting of Mash2, a mouse gene required for trophoblast development | Q38298288 | ||
| Epigenetic regulation of gene expression: the effect of altered chromatin structure from yeast to mammals | Q40934967 | ||
| Mutations in the gene encoding fibroblast growth factor receptor-3 in achondroplasia | Q45345175 | ||
| Genetic imprinting in the mouse: implications for gene regulation. | Q52220346 | ||
| Relaxation of imprinted genes in human cancer. | Q52545355 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans | Q58061470 | ||
| A new genetic concept: uniparental disomy and its potential effect, isodisomy | Q70656134 | ||
| Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation | Q71953304 | ||
| Sex-specific meiotic recombination in the Prader--Willi/Angelman syndrome imprinted region | Q71953399 | ||
| Parental genomic imprinting of the human IGF2 gene | Q72222239 | ||
| Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour | Q72703028 | ||
| Epigenetic lesions at the H19 locus in Wilms' tumour patients | Q72703033 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 95-98 | |
| P577 | publication date | 1997-05-01 | |
| P1433 | published in | American Journal of Medical Genetics Part A | Q15755121 |
| P1476 | title | Imprinting is also a mechanism for immediate or delayed hemizygous expression of several uniparental haplotypes selected from the genome of each sex. | |
| P478 | volume | 70 |
| Q27006276 | Coadaptation and conflict, misconception and muddle, in the evolution of genomic imprinting | cites work | P2860 |
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