Compounds > tryptophan

tryptophan and Cleidocranial Digital Dysostosis

tryptophan has been researched along with Cleidocranial Digital Dysostosis in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, QY; Fu, DJ; Li, J; Liu, ZM; Mao, TT; Peng, YJ; She, WT1
Bertini, E; Dionisi-Vici, C; Florio, LD; Giannotti, A; Patrono, C; Santorelli, FM; Tessa, A; Velardo, M1
Hasegawa, H; Hirose, R; Sakai, N; Susami, T; Takato, T; Tokunaga, K; Uchinuma, E; Ui, K; Yamazaki, Y1

Other Studies

3 other study(ies) available for tryptophan and Cleidocranial Digital Dysostosis

ArticleYear
A novel gene mutation of Runx2 in cleidocranial dysplasia.
    Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban, 2017, Volume: 37, Issue:5

    Topics: Adult; Amino Acid Substitution; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Exons; Female; Genetic Predisposition to Disease; Histidine; Humans; Mutation, Missense; Pedigree; Sequence Analysis, DNA; Tryptophan

2017
A novel CBFA1 mutation (R190W) in an Italian family with cleidocranial dysplasia.
    Human mutation, 2000, Volume: 16, Issue:3

    Topics: Amino Acid Substitution; Arginine; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Humans; Italy; Mutation, Missense; Neoplasm Proteins; Transcription Factors; Tryptophan

2000
A case of a Japanese patient with cleidocranial dysplasia possessing a mutation of CBFA1 gene.
    The Journal of craniofacial surgery, 2002, Volume: 13, Issue:1

    Topics: Aged; Amino Acid Substitution; Arginine; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Core Binding Factors; DNA Mutational Analysis; Humans; Japan; Male; Mutation, Missense; Neoplasm Proteins; Transcription Factors; Tryptophan

2002