Page last updated: 2024-08-23

transferrin and Labhart-Willi Syndrome

transferrin 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	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
Bowling, FG; Heussler, HS; Munce, T	1

Other Studies

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

Article	Year
Analysis of N- and O-linked protein glycosylation in children with Prader-Willi syndrome. Journal of intellectual disability research : JIDR, 2010, Volume: 54, Issue:10 Topics: Adolescent; Apolipoprotein C-III; Child; Child, Preschool; Genotype; Glycoproteins; Glycosylation; Humans; Infant; Infant, Newborn; Isoelectric Focusing; N-Acetylneuraminic Acid; Phenotype; Prader-Willi Syndrome; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Transferrin; Young Adult	2010

Article

Year

Analysis of N- and O-linked protein glycosylation in children with Prader-Willi syndrome.

Journal of intellectual disability research : JIDR, 2010, Volume: 54, Issue:10

Topics: Adolescent; Apolipoprotein C-III; Child; Child, Preschool; Genotype; Glycoproteins; Glycosylation; Humans; Infant; Infant, Newborn; Isoelectric Focusing; N-Acetylneuraminic Acid; Phenotype; Prader-Willi Syndrome; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Transferrin; Young Adult

2010