propiconazole has been researched along with Chromosome Deletion in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (20.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bajaj, MS; Bhadange, Y; Chandra, M; Chawla, B; Dada, R; Ghose, S; Kumar, M; Pushker, N; Sharma, S | 1 |
Aaberg, TM; Droste, PJ; Hassan, AS; Pearce, ZD | 1 |
Chaker, A; Hoffmann, TK; Ramp, U; Scheckenbach, K; Wagenmann, M; Winterhalter, S | 1 |
Allanson, J; Richter, S | 1 |
Emanuel, BS; Münke, M; Zackai, EH | 1 |
2 review(s) available for propiconazole and Chromosome Deletion
Article | Year |
---|---|
Ophthalmic and systemic findings in interstitial deletions of chromosome 14q: a case report and literature review.
Topics: Abnormalities, Multiple; Anophthalmos; Chromosome Deletion; Chromosomes, Human, Pair 14; Coloboma; Electroretinography; Eye Abnormalities; Eyelids; Female; Humans; Infant, Newborn; Iris; Magnetic Resonance Imaging; Microphthalmos; Orbit; Retina; Tomography, Optical Coherence; Tomography, X-Ray Computed | 2012 |
Holoprosencephaly: association with interstitial deletion of 2p and review of the cytogenetic literature.
Topics: Abnormalities, Multiple; Brain; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 2; Female; Humans; Infant, Newborn; Orbit | 1988 |
3 other study(ies) available for propiconazole and Chromosome Deletion
Article | Year |
---|---|
Clinical, radiologic, and genetic features in blepharophimosis, ptosis, and epicanthus inversus syndrome in the Indian population.
Topics: Adolescent; Adult; Amblyopia; Blepharophimosis; Case-Control Studies; Child; Child, Preschool; Chromosome Deletion; Chromosomes, Human, Pair 3; Eyelids; Female; Forkhead Box Protein L2; Forkhead Transcription Factors; Humans; India; Male; Mutation; Orbit; Refractive Errors; Strabismus; Syndrome; Tomography, X-Ray Computed; Young Adult | 2013 |
[MALT lymphoma of the orbit].
Topics: Aged; Antigens, CD20; Biopsy; CD3 Complex; Chromosome Aberrations; Chromosome Deletion; Chromosomes, Human, Pair 11; Diagnosis, Differential; Diplopia; Dose Fractionation, Radiation; Endoscopy; Exophthalmos; Female; Follow-Up Studies; Humans; Ki-67 Antigen; Lymphoma, B-Cell, Marginal Zone; Magnetic Resonance Imaging; Neoplasm Staging; Oculomotor Muscles; Orbit; Orbital Neoplasms | 2008 |
Linear skin defects and congenital microphthalmia: a new syndrome at Xp22.2.
Topics: Adult; Chromosome Deletion; Female; Humans; Infant, Newborn; Microphthalmos; Orbit; Pigmentation Disorders; Sex Chromosome Aberrations; Skin Abnormalities; Syndrome; X Chromosome | 1991 |