Page last updated: 2024-08-26

hydrogen sulfite and Syndrome

hydrogen sulfite has been researched along with Syndrome 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
Adam, MP; Akkari, YM; Anadiotis, G; Bamshad, MJ; Baratela, WAR; Bober, MB; Dempsey, JC; Doherty, D; Duker, AL; Fagerstrom, C; Gripp, KW; Kernan, K; Kircher, M; LaCroix, AJ; Mefford, HC; Mehaffey, M; Miller, DG; Myers, CT; Nickerson, DA; Robbins, KM; Sahraoui, R; Sol-Church, K; Stabley, D	1

Other Studies

1 other study(ies) available for hydrogen sulfite and Syndrome

Article	Year
GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome. American journal of human genetics, 2019, 01-03, Volume: 104, Issue:1 Topics: Abnormalities, Multiple; Alleles; Blotting, Southern; Cohort Studies; DNA Methylation; Epigenesis, Genetic; Exons; Female; Humans; Infant; Infant, Newborn; Male; Mutation; Pedigree; Pentosyltransferases; Sulfites; Syndrome; Trinucleotide Repeat Expansion; UDP Xylose-Protein Xylosyltransferase	2019

Article

Year

GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome.

American journal of human genetics, 2019, 01-03, Volume: 104, Issue:1

Topics: Abnormalities, Multiple; Alleles; Blotting, Southern; Cohort Studies; DNA Methylation; Epigenesis, Genetic; Exons; Female; Humans; Infant; Infant, Newborn; Male; Mutation; Pedigree; Pentosyltransferases; Sulfites; Syndrome; Trinucleotide Repeat Expansion; UDP Xylose-Protein Xylosyltransferase

2019