These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
45. Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting. Kotzot D Ann Genet; 2004; 47(3):251-60. PubMed ID: 15337470 [TBL] [Abstract][Full Text] [Related]
46. Relaxation of IGF2 imprinting in Wilms tumours associated with specific changes in IGF2 methylation. Sullivan MJ; Taniguchi T; Jhee A; Kerr N; Reeve AE Oncogene; 1999 Dec; 18(52):7527-34. PubMed ID: 10602511 [TBL] [Abstract][Full Text] [Related]
47. No evidence for large-scale germline genomic aberrations in hereditary bladder cancer patients with high-resolution array-based comparative genomic hybridization. Kiemeney LA; Kuiper RP; Pfundt R; van Reijmersdal S; Schoenberg MP; Aben KK; Niermeijer MF; Witjes JA; Schoenmakers EF Cancer Epidemiol Biomarkers Prev; 2006 Jan; 15(1):180-3. PubMed ID: 16434610 [No Abstract] [Full Text] [Related]
48. Genomic imprinting and reproduction. Swales AK; Spears N Reproduction; 2005 Oct; 130(4):389-99. PubMed ID: 16183857 [TBL] [Abstract][Full Text] [Related]
49. [Hereditary chromosomal mosaicism and its importance for the affected family]. Zdansky R; Madl W; Rett A; Piperger A Wien Med Wochenschr; 1971 Jan; 121(4):59-63. PubMed ID: 4252342 [No Abstract] [Full Text] [Related]
51. Genomic imprinting at the WT1 gene involves a novel coding transcript (AWT1) that shows deregulation in Wilms' tumours. Dallosso AR; Hancock AL; Brown KW; Williams AC; Jackson S; Malik K Hum Mol Genet; 2004 Feb; 13(4):405-15. PubMed ID: 14681303 [TBL] [Abstract][Full Text] [Related]
52. Analysis of the spectrum of malformations in human fetuses of the second and third trimester of pregnancy with human triploidy. Sergi C; Schiesser M; Adam S; Otto HF Pathologica; 2000 Aug; 92(4):257-63. PubMed ID: 11029886 [TBL] [Abstract][Full Text] [Related]
53. The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age. Ginsburg C; Fokstuen S; Schinzel A Am J Med Genet; 2000 Dec; 95(5):454-60. PubMed ID: 11146466 [TBL] [Abstract][Full Text] [Related]
58. [Regional characteristics of the incidence of hereditary pathology in Uzbekistan]. Gar'kavtseva RF; Ginter EK; Revazov AA Vestn Akad Med Nauk SSSR; 1984; (7):69-75. PubMed ID: 6236633 [No Abstract] [Full Text] [Related]
59. How imprinting is relevant to human disease. Hall JG Dev Suppl; 1990; ():141-8. PubMed ID: 2090424 [TBL] [Abstract][Full Text] [Related]