tryptophan and Congenital Foot Deformities

tryptophan has been researched along with Congenital Foot Deformities in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM	1
Kneppers, A; Passos-Bueno, MR; Richieri-Costa, A; Sertié, AL	1

Other Studies

2 other study(ies) available for tryptophan and Congenital Foot Deformities

Article	Year
Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5 Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female; Foot Deformities, Congenital; Genotype; Hand Deformities, Congenital; Heterozygote; Humans; Melanosis; Mutation, Missense; Phenotype; Sequence Analysis, Protein; Thymine; Transcription Factors; Tryptophan; Tumor Suppressor Proteins	2010
Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactyly. Journal of medical genetics, 1998, Volume: 35, Issue:8 Topics: Acrocephalosyndactylia; Child, Preschool; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Mutation; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Serine; Syndactyly; Tryptophan	1998

Article

Year

Ectrodactyly-ectodermal dysplasia-clefting syndrome associated with p63 mutation and an uncommon phenotype.

The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association, 2010, Volume: 47, Issue:5

Topics: Adolescent; Arginine; Cleft Lip; Cleft Palate; Codon; Cytosine; Ectodermal Dysplasia; Exons; Female; Foot Deformities, Congenital; Genotype; Hand Deformities, Congenital; Heterozygote; Humans; Melanosis; Mutation, Missense; Phenotype; Sequence Analysis, Protein; Thymine; Transcription Factors; Tryptophan; Tumor Suppressor Proteins

2010

Presence of the Apert canonical S252W FGFR2 mutation in a patient without severe syndactyly.

Journal of medical genetics, 1998, Volume: 35, Issue:8

Topics: Acrocephalosyndactylia; Child, Preschool; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Mutation; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Serine; Syndactyly; Tryptophan

1998