histidine has been researched along with Craniofacial Abnormalities in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Brown, CA; Lupski, JR; Potocki, L; Shen, JJ | 1 |
1 other study(ies) available for histidine and Craniofacial Abnormalities
Article | Year |
---|---|
Mandibuloacral dysplasia caused by homozygosity for the R527H mutation in lamin A/C.
Topics: Abnormalities, Multiple; Adolescent; Amino Acid Substitution; Arginine; Craniofacial Abnormalities; Genes, Recessive; Genotype; Histidine; Homozygote; Humans; Lamin Type A; Lipodystrophy; Male; Musculoskeletal Abnormalities; Mutation; Phenotype | 2003 |