| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Lewis SE | |
| Erickson RP | |||
| P2860 | cites work | Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A | Q28117400 |
| Genomic imprinting in mammalian development: a parental tug-of-war | Q28278146 | ||
| Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy | Q28292821 | ||
| Properties and localization of DNA methyltransferase in preimplantation mouse embryos: implications for genomic imprinting | Q31161773 | ||
| Chromosome imprinting and the mammalian X chromosome | Q33966462 | ||
| Development of reconstituted mouse eggs suggests imprinting of the genome during gametogenesis | Q34056205 | ||
| Preferential inactivation of the paternally derived X chromosome in the extraembryonic membranes of the mouse | Q34088761 | ||
| Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy | Q34231877 | ||
| Completion of mouse embryogenesis requires both the maternal and paternal genomes | Q34267351 | ||
| Inviability of parthenogenones is determined by pronuclei, not egg cytoplasm | Q34267797 | ||
| Structural clues to prion replication | Q34322278 | ||
| Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. | Q34353488 | ||
| Trinucleotide repeat length instability and age of onset in Huntington's disease | Q34357407 | ||
| Methylation and imprinting: from host defense to gene regulation? | Q34363070 | ||
| Uniparental paternal disomy in a genetic cancer-predisposing syndrome | Q34535432 | ||
| The role of X-chromosome inactivation during spermatogenesis (Drosophila-allocycly-chromosome evolution-male sterility-dosage compensation). | Q34768106 | ||
| The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus | Q34776140 | ||
| Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions | Q36759870 | ||
| A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues | Q37147048 | ||
| Familiarity, recessivity and germline mosaicism | Q38639759 | ||
| Uniparental disomy and genomic imprinting as causes of human genetic disease | Q40549875 | ||
| Isolation of an active human transposable element | Q42614185 | ||
| Recurrence of lethal osteogenesis imperfecta due to parental mosaicism for a mutation in the COL1A2 gene of type I collagen. The mosaic parent exhibits phenotypic features of a mild form of the disease | Q46953870 | ||
| Instability of short tandem repeats (microsatellites) in human cancers. | Q48181678 | ||
| A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies | Q48836050 | ||
| Glucose-6-phosphate dehydrogenase activity changes during spermatogenesis: possible relevance to X-chromosome inactivation | Q50863259 | ||
| Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. | Q52034632 | ||
| The marker (X) syndrome: a cytogenetic and genetic analysis. | Q52093239 | ||
| Cell surfaces and embryos: expression of the F9 teratocarcinoma antigen in T-region lethal, other lethal, and normal pre-implantation mouse embryos. | Q52296255 | ||
| Parental imprinting of the mouse insulin-like growth factor II gene. | Q55052428 | ||
| Maternal T hp lethality in the mouse is a nuclear, not cytoplasmic, defect | Q59061949 | ||
| One gene—four syndromes | Q59096823 | ||
| Preferential expression of the maternally derived X chromosome in the mouse yolk sac | Q62555376 | ||
| Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion | Q67482157 | ||
| Unstable DNA sequence in myotonic dystrophy | Q67516021 | ||
| Familial mitochondrial encephalomyopathy (MERRF): genetic, pathophysiological, and biochemical characterization of a mitochondrial DNA disease | Q67950234 | ||
| Some milestones in the history of X-chromosome inactivation | Q67986532 | ||
| Further observations on the haipin-tail (Thp) mutation in the mouse | Q68880061 | ||
| The infectious nature of prions | Q69951458 | ||
| Genetic mosaicism in normal tissues of Wilms' tumour patients | Q70457181 | ||
| Differences in the DNA of the inactive X chromosomes of fetal and extraembryonic tissues of mice | Q71219235 | ||
| P921 | main subject | human genetics | Q265799 |
| P304 | page(s) | 7-12 | |
| P577 | publication date | 1995-01-01 | |
| P1433 | published in | Environmental and Molecular Mutagenesis | Q15724469 |
| P1476 | title | The new human genetics | |
| P478 | volume | 25 Suppl 26 |
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