Page last updated: 2024-08-22

trolamine salicylate and Absence of Corpus Callosum

trolamine salicylate has been researched along with Absence of Corpus Callosum 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
Claes, C; Collins, F; Flaherty, M; Pinner, J; Schrauwen, I; Sommen, M; Van Camp, G	1

Other Studies

1 other study(ies) available for trolamine salicylate and Absence of Corpus Callosum

Article	Year
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome. Clinical genetics, 2014, Volume: 86, Issue:3 Topics: Agenesis of Corpus Callosum; Arthritis; Base Sequence; Collagen Diseases; Connective Tissue Diseases; Eye; Hearing Loss, Sensorineural; Hernias, Diaphragmatic, Congenital; Humans; Low Density Lipoprotein Receptor-Related Protein-2; Magnetic Resonance Imaging; Molecular Sequence Data; Mutation, Missense; Myopia; Pedigree; Phenotype; Proteinuria; Renal Tubular Transport, Inborn Errors; Retinal Detachment; Sequence Analysis, DNA	2014

Article

Year

Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome.

Clinical genetics, 2014, Volume: 86, Issue:3

Topics: Agenesis of Corpus Callosum; Arthritis; Base Sequence; Collagen Diseases; Connective Tissue Diseases; Eye; Hearing Loss, Sensorineural; Hernias, Diaphragmatic, Congenital; Humans; Low Density Lipoprotein Receptor-Related Protein-2; Magnetic Resonance Imaging; Molecular Sequence Data; Mutation, Missense; Myopia; Pedigree; Phenotype; Proteinuria; Renal Tubular Transport, Inborn Errors; Retinal Detachment; Sequence Analysis, DNA

2014