arginine and Franceschetti-Zwahlen-Klein Syndrome

arginine 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; Igawa, H; Kawashima, K; Sakiyama, Y; Sugihara, T; Yamamoto, Y	1

Other Studies

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

Article	Year
Treacher Collins syndrome with craniosynostosis, choanal atresia, and esophageal regurgitation caused by a novel nonsense mutation in TCOF1. American journal of medical genetics. Part A, 2004, Jul-15, Volume: 128A, Issue:2 Topics: Arginine; Child, Preschool; Codon, Nonsense; Codon, Terminator; Craniosynostoses; DNA Mutational Analysis; Exons; Facies; Female; Gastroesophageal Reflux; Gene Deletion; Humans; Mandibulofacial Dysostosis; Mutation; Nuclear Proteins; Phosphoproteins; Polymorphism, Single-Stranded Conformational; Tomography, X-Ray Computed	2004

Article

Year

Treacher Collins syndrome with craniosynostosis, choanal atresia, and esophageal regurgitation caused by a novel nonsense mutation in TCOF1.

American journal of medical genetics. Part A, 2004, Jul-15, Volume: 128A, Issue:2

Topics: Arginine; Child, Preschool; Codon, Nonsense; Codon, Terminator; Craniosynostoses; DNA Mutational Analysis; Exons; Facies; Female; Gastroesophageal Reflux; Gene Deletion; Humans; Mandibulofacial Dysostosis; Mutation; Nuclear Proteins; Phosphoproteins; Polymorphism, Single-Stranded Conformational; Tomography, X-Ray Computed

2004