threonine and Craniofacial Abnormalities

threonine has been researched along with Craniofacial Abnormalities in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Coletta, RD; Line, SR; Martelli-Júnior, H; Oliveira Swerts, MS; Paranaíba, LM	1
Feng, H; Wang, Y; Zhang, X; Zhao, H	1

Other Studies

2 other study(ies) available for threonine and Craniofacial Abnormalities

Article	Year
Novel mutations in the IRF6 gene in Brazilian families with Van der Woude syndrome. International journal of molecular medicine, 2008, Volume: 22, Issue:4 Topics: Alanine; American Indian or Alaska Native; Amino Acid Sequence; Base Sequence; Brazil; Craniofacial Abnormalities; DNA Mutational Analysis; Electrophoresis, Agar Gel; Family; Humans; Interferon Regulatory Factors; Molecular Sequence Data; Mutation; Restriction Mapping; Syndrome; Threonine	2008
Novel identification of a four-base-pair deletion mutation in PITX2 in a Rieger syndrome family. Journal of dental research, 2003, Volume: 82, Issue:12 Topics: Adolescent; Adult; Aged; Anodontia; Base Pairing; Base Sequence; Child; China; Codon, Terminator; Craniofacial Abnormalities; Exons; Female; Frameshift Mutation; Homeobox Protein PITX2; Homeodomain Proteins; Humans; Male; Mutation; Pedigree; Phenotype; Sequence Deletion; Syndrome; Threonine; Tooth Abnormalities; Transcription Factors	2003

Article

Year

Novel mutations in the IRF6 gene in Brazilian families with Van der Woude syndrome.

International journal of molecular medicine, 2008, Volume: 22, Issue:4

Topics: Alanine; American Indian or Alaska Native; Amino Acid Sequence; Base Sequence; Brazil; Craniofacial Abnormalities; DNA Mutational Analysis; Electrophoresis, Agar Gel; Family; Humans; Interferon Regulatory Factors; Molecular Sequence Data; Mutation; Restriction Mapping; Syndrome; Threonine

2008

Novel identification of a four-base-pair deletion mutation in PITX2 in a Rieger syndrome family.

Journal of dental research, 2003, Volume: 82, Issue:12

Topics: Adolescent; Adult; Aged; Anodontia; Base Pairing; Base Sequence; Child; China; Codon, Terminator; Craniofacial Abnormalities; Exons; Female; Frameshift Mutation; Homeobox Protein PITX2; Homeodomain Proteins; Humans; Male; Mutation; Pedigree; Phenotype; Sequence Deletion; Syndrome; Threonine; Tooth Abnormalities; Transcription Factors

2003