cysteine has been researched along with Congenital Hand Deformities in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 3 (100.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Diaz-Valdez, M; Falasca, GF; Jimenez, SA; Neumann, G; Passano, GM; Reginato, AJ; Williams, CJ | 1 |
Costa, T; Erlacher, L; Kilpatrick, MW; Lembessis, P; Lin, K; Luyten, FP; Thomas, JT; Tsipouras, P | 1 |
Bartlett, SP; Gripp, KW; Katowitz, JA; Markowitz, RI; McDonald-McGinn, DM; Muenke, M; Stolle, CA; Zackai, EH | 1 |
3 other study(ies) available for cysteine and Congenital Hand Deformities
Article | Year |
---|---|
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
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.
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.
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 |