tridemorph has been researched along with Abnormalities, Autosome in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (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 |
---|---|
Bullrich, F; Czarnecki, P; Pulkkinen, L; Uitto, J; Weiss, L | 1 |
Hagiwara, S; Lin, L; Nishikawa, T; Pulkkinen, L; Shimizu, H; Takizawa, Y; Uitto, J | 1 |
2 other study(ies) available for tridemorph and Abnormalities, Autosome
Article | Year |
---|---|
Maternal uniparental disomy of chromosome 1 with reduction to homozygosity of the LAMB3 locus in a patient with Herlitz junctional epidermolysis bullosa.
Topics: Alleles; Cell Adhesion Molecules; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 1; Epidermolysis Bullosa, Junctional; Female; Haplotypes; Heterozygote; Homozygote; Humans; Infant, Newborn; Kalinin; Male; Pedigree; Point Mutation | 1997 |
Maternal uniparental meroisodisomy in the LAMB3 region of chromosome 1 results in lethal junctional epidermolysis bullosa.
Topics: Cell Adhesion Molecules; Chromosome Aberrations; Chromosomes, Human, Pair 1; Epidermolysis Bullosa, Junctional; Fatal Outcome; Female; Genotype; Homozygote; Humans; Infant, Newborn; Kalinin; Maternal-Fetal Exchange; Mutation; Pregnancy | 1998 |