Page last updated: 2024-08-18

isomethyleugenol and Congenital Hypothyroidism

isomethyleugenol has been researched along with Congenital Hypothyroidism in 1 studies

Research

Studies (1)

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

Authors

Authors	Studies
Higashimoto, K; Ihara, K; Imagawa, E; Matsumoto, N; Matsunaga, S; Miyake, N; Miyatake, S; Mizuguchi, T; Nakashima, M; Nishimura, G; Numakura, C; Okamoto, N; Ryo, A; Saitsu, H; Sakai, Y; Sanefuji, M; Sato, Y; Soejima, H; Takada, Y	1

Other Studies

1 other study(ies) available for isomethyleugenol and Congenital Hypothyroidism

Article	Year
Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome. Human mutation, 2017, Volume: 38, Issue:6 Topics: Abnormalities, Multiple; Adult; Child; Child, Preschool; Congenital Hypothyroidism; Craniofacial Abnormalities; Cullin Proteins; DNA-Binding Proteins; Enhancer of Zeste Homolog 2 Protein; Female; Hand Deformities, Congenital; Heterozygote; Histones; Humans; Male; Methylation; Mutation; Neoplasm Proteins; Pedigree; Polycomb Repressive Complex 2; Protein Interaction Maps; Transcription Factors	2017

Article

Year

Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.

Human mutation, 2017, Volume: 38, Issue:6

Topics: Abnormalities, Multiple; Adult; Child; Child, Preschool; Congenital Hypothyroidism; Craniofacial Abnormalities; Cullin Proteins; DNA-Binding Proteins; Enhancer of Zeste Homolog 2 Protein; Female; Hand Deformities, Congenital; Heterozygote; Histones; Humans; Male; Methylation; Mutation; Neoplasm Proteins; Pedigree; Polycomb Repressive Complex 2; Protein Interaction Maps; Transcription Factors

2017