Compounds > cysteine

cysteine and Congenital Hand Deformities

cysteine 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's3 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Diaz-Valdez, M; Falasca, GF; Jimenez, SA; Neumann, G; Passano, GM; Reginato, AJ; Williams, CJ1
Costa, T; Erlacher, L; Kilpatrick, MW; Lembessis, P; Lin, K; Luyten, FP; Thomas, JT; Tsipouras, P1
Bartlett, SP; Gripp, KW; Katowitz, JA; Markowitz, RI; McDonald-McGinn, DM; Muenke, M; Stolle, CA; Zackai, EH1

Other Studies

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

ArticleYear
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
Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1.
    Nature genetics, 1997, Volume: 17, Issue:1

    Topics: Amino Acid Sequence; Animals; Base Sequence; Bone Morphogenetic Proteins; Conserved Sequence; COS Cells; Cysteine; Dwarfism; Female; Fingers; Genes, Dominant; Genes, Recessive; Growth Differentiation Factor 5; Growth Substances; Hand Deformities, Congenital; Heterozygote; Humans; Male; Morphogenesis; Osteochondrodysplasias; Pedigree; Point Mutation; Recombinant Proteins; Transfection; Tyrosine

1997
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type III.
    American journal of medical genetics, 1998, Jul-24, Volume: 78, Issue:4

    Topics: Abnormalities, Multiple; Acrocephalosyndactylia; Amino Acid Substitution; Cysteine; Elbow; Eye Abnormalities; Foot Deformities, Congenital; Hand Deformities, Congenital; Humans; Infant, Newborn; Male; Phenotype; Point Mutation; Polymorphism, Single-Stranded Conformational; Radiography; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 2; Receptors, Fibroblast Growth Factor; Serine; Translocation, Genetic; Wheelchairs

1998