Page last updated: 2024-08-23

propiconazole and Chromosome Deletion

propiconazole has been researched along with Chromosome Deletion in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bajaj, MS; Bhadange, Y; Chandra, M; Chawla, B; Dada, R; Ghose, S; Kumar, M; Pushker, N; Sharma, S1
Aaberg, TM; Droste, PJ; Hassan, AS; Pearce, ZD1
Chaker, A; Hoffmann, TK; Ramp, U; Scheckenbach, K; Wagenmann, M; Winterhalter, S1
Allanson, J; Richter, S1
Emanuel, BS; Münke, M; Zackai, EH1

Reviews

2 review(s) available for propiconazole and Chromosome Deletion

ArticleYear
Ophthalmic and systemic findings in interstitial deletions of chromosome 14q: a case report and literature review.
    Ophthalmic genetics, 2012, Volume: 33, Issue:3

    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.
    American journal of medical genetics, 1988, Volume: 30, Issue:4

    Topics: Abnormalities, Multiple; Brain; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, Pair 2; Female; Humans; Infant, Newborn; Orbit

1988

Other Studies

3 other study(ies) available for propiconazole and Chromosome Deletion

ArticleYear
Clinical, radiologic, and genetic features in blepharophimosis, ptosis, and epicanthus inversus syndrome in the Indian population.
    Investigative ophthalmology & visual science, 2013, Apr-26, Volume: 54, Issue:4

    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].
    HNO, 2008, Volume: 56, Issue:2

    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.
    Journal of medical genetics, 1991, Volume: 28, Issue:2

    Topics: Adult; Chromosome Deletion; Female; Humans; Infant, Newborn; Microphthalmos; Orbit; Pigmentation Disorders; Sex Chromosome Aberrations; Skin Abnormalities; Syndrome; X Chromosome

1991