Page last updated: 2024-08-17

bromodeoxyuridine and Labhart-Willi Syndrome

bromodeoxyuridine has been researched along with Labhart-Willi Syndrome in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Gartler, SM; Hansen, RS; Kawame, H	1

Other Studies

1 other study(ies) available for bromodeoxyuridine and Labhart-Willi Syndrome

Article	Year
Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci. Human molecular genetics, 1995, Volume: 4, Issue:12 Topics: Alleles; Autoantigens; Base Sequence; Bromodeoxyuridine; Cell Line, Transformed; DNA; DNA Replication; Genomic Imprinting; HeLa Cells; Humans; In Situ Hybridization, Fluorescence; Insulin-Like Growth Factor II; Molecular Sequence Data; Muscle Proteins; Prader-Willi Syndrome; Ribonucleoproteins, Small Nuclear; RNA, Long Noncoding; RNA, Untranslated; Sequence Tagged Sites; snRNP Core Proteins; Time Factors	1995

Article

Year

Allele-specific replication timing in imprinted domains: absence of asynchrony at several loci.

Human molecular genetics, 1995, Volume: 4, Issue:12

Topics: Alleles; Autoantigens; Base Sequence; Bromodeoxyuridine; Cell Line, Transformed; DNA; DNA Replication; Genomic Imprinting; HeLa Cells; Humans; In Situ Hybridization, Fluorescence; Insulin-Like Growth Factor II; Molecular Sequence Data; Muscle Proteins; Prader-Willi Syndrome; Ribonucleoproteins, Small Nuclear; RNA, Long Noncoding; RNA, Untranslated; Sequence Tagged Sites; snRNP Core Proteins; Time Factors

1995