Compounds > arginine

arginine and Congenital Hand Deformities

arginine has been researched along with Congenital Hand Deformities in 3 studies

Research

Studies (3)

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

Authors

AuthorsStudies
Abdo Filho, RC; Bufalino, A; Coletta, RD; de Miranda, RT; Martelli-Júnior, H; Paranaíba, LM1
Diaz-Valdez, M; Falasca, GF; Jimenez, SA; Neumann, G; Passano, GM; Reginato, AJ; Williams, CJ1
Braddock, SR; Graham, JM; Jabs, EW; Lachman, R; Mortier, GR; Van Dop, C1

Other Studies

3 other study(ies) available for arginine and Congenital Hand Deformities

ArticleYear
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
Familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis associated with an arginine 75-->cysteine mutation in the procollagen type II gene in a kindred of Chiloe Islanders. I. Clinical, radiographic, and pathologic findin
    Arthritis and rheumatism, 1994, Volume: 37, Issue:7

    Topics: Adult; Arginine; Chile; Cysteine; DNA; Female; Foot Deformities, Congenital; Hand; Hand Deformities, Congenital; Hip; Humans; Knee; Leukocytes; Osteoarthritis; Osteochondrodysplasias; Pedigree; Point Mutation; Polymerase Chain Reaction; Procollagen; Radiography

1994
Syndrome of coronal craniosynostosis with brachydactyly and carpal/tarsal coalition due to Pro250Arg mutation in FGFR3 gene.
    American journal of medical genetics, 1998, May-26, Volume: 77, Issue:4

    Topics: Abnormalities, Multiple; Adolescent; Arginine; Craniosynostoses; DNA Mutational Analysis; Female; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Infant; Male; Pedigree; Point Mutation; Proline; Protein-Tyrosine Kinases; Radiography; Receptor, Fibroblast Growth Factor, Type 3; Receptors, Fibroblast Growth Factor; Syndrome

1998