propiconazole has been researched along with Autosomal Chromosome Disorders in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (80.00) | 18.7374 |
1990's | 1 (20.00) | 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 |
---|---|
Bartley, JA; Jacoby, CG; Judisch, GF; Kraft, SP | 1 |
Bahlmann, F; Merz, E; PĆ¼ttmann, S; Weber, G; Wellek, S | 1 |
Hennigar, GR; Osborne, RA; Singh, DN; Wiscovitch, RA | 1 |
Capitanio, MA; Kirkpatrick, JA | 1 |
Moragas, A; Prats, J | 1 |
5 other study(ies) available for propiconazole and Autosomal Chromosome Disorders
Article | Year |
---|---|
Orbital hypotelorism. An isolated autosomal dominant trait.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Ethmoid Bone; Female; Genes, Dominant; Humans; Male; Middle Aged; Orbit; Pedigree | 1984 |
[Orbital diameter, inner and outer orbital distance. A growth model of fetal orbital measurements].
Topics: Cephalometry; Chromosome Aberrations; Chromosome Disorders; Cross-Sectional Studies; Embryonic and Fetal Development; Female; Gestational Age; Humans; Infant, Newborn; Male; Orbit; Pregnancy; Prospective Studies; Reference Values; Ultrasonography, Prenatal | 1995 |
Partial trisomy 13 in a case of Cyclopia with 13-14 translocation.
Topics: Abnormalities, Multiple; Autopsy; Brain Stem; Cells, Cultured; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, 13-15; Ear; Eye Abnormalities; Humans; Infant, Newborn; Karyotyping; Lymphocytes; Male; Microscopy, Fluorescence; Orbit; Syndrome; Trisomy | 1974 |
Radiology of the orbit in infancy and childhood.
Topics: Achondroplasia; Anemia, Hemolytic; Calcinosis; Child; Chromosome Aberrations; Chromosome Disorders; Encephalocele; Hemangioma; Humans; Hydrocephalus; Hyperostosis, Cortical, Congenital; Infant, Newborn; Infant, Newborn, Diseases; Microcephaly; Mucocele; Neoplasm Metastasis; Orbit; Orbital Neoplasms; Osteomyelitis; Osteopetrosis; Radiography; Retinoblastoma; Rhabdomyosarcoma; Skull Fractures; Wilms Tumor | 1972 |
Structural chromosome anomaly in a case of multiple malformation.
Topics: Abnormalities, Multiple; Adult; Autopsy; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Face; Female; Humans; Infant, Newborn; Kidney; Lung; Male; Orbit; Pregnancy; Trisomy | 1967 |