valine and Franceschetti-Zwahlen-Klein Syndrome

valine has been researched along with Franceschetti-Zwahlen-Klein 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	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Ariga, T; Fujioka, H; Horiuchi, K; Ishikiriyama, S; Kawashima, K; Otsu, M; Oyama, K; Sakiyama, Y; Sugihara, T; Yamamoto, Y	1

Other Studies

1 other study(ies) available for valine and Franceschetti-Zwahlen-Klein Syndrome

Article	Year
Detection of a novel silent deletion, a missense mutation and a nonsense mutation in TCOF1. Pediatrics international : official journal of the Japan Pediatric Society, 2008, Volume: 50, Issue:6 Topics: Adolescent; Adult; Alanine; Codon, Nonsense; Frameshift Mutation; Humans; Infant; Lysine; Mandibulofacial Dysostosis; Mutation, Missense; Nuclear Proteins; Pedigree; Phosphoproteins; Polymorphism, Single-Stranded Conformational; Reverse Transcriptase Polymerase Chain Reaction; Sequence Deletion; Valine	2008

Article

Year

Detection of a novel silent deletion, a missense mutation and a nonsense mutation in TCOF1.

Pediatrics international : official journal of the Japan Pediatric Society, 2008, Volume: 50, Issue:6

Topics: Adolescent; Adult; Alanine; Codon, Nonsense; Frameshift Mutation; Humans; Infant; Lysine; Mandibulofacial Dysostosis; Mutation, Missense; Nuclear Proteins; Pedigree; Phosphoproteins; Polymorphism, Single-Stranded Conformational; Reverse Transcriptase Polymerase Chain Reaction; Sequence Deletion; Valine

2008