Page last updated: 2024-10-20

thymine and Eye Abnormalities

thymine has been researched along with Eye Abnormalities in 5 studies

Eye Abnormalities: Congenital absence of or defects in structures of the eye; may also be hereditary.

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (60.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Qin, W1
Lu, X1
Lin, S1
Zhou, G1
Zhou, N1
Hu, S1
Zhao, L1
Zhang, C1
Qi, Y1
Vanita, V1
Singh, JR1
Hejtmancik, JF1
Nuernberg, P1
Hennies, HC1
Singh, D1
Sperling, K1
Wang, J1
Liu, J1
Zhang, Q1
Meyer-Marcotty, P1
Weisschuh, N1
Dressler, P1
Hartmann, J1
Stellzig-Eisenhauer, A1

Other Studies

5 other studies available for thymine and Eye Abnormalities

ArticleYear
Programmable base editing in zebrafish using a modified CRISPR-Cas9 system.
    Methods (San Diego, Calif.), 2018, 11-01, Volume: 150

    Topics: Abnormalities, Multiple; Animals; Base Sequence; CRISPR-Cas Systems; Cytidine; Cytidine Deaminase; D

2018
A missense mutation in CRYBA4 associated with congenital cataract and microcornea.
    Molecular vision, 2010, Jun-05, Volume: 16

    Topics: Adolescent; Adult; Amino Acid Substitution; Base Sequence; beta-Crystallin A Chain; Cataract; Child;

2010
A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.
    Molecular vision, 2006, May-22, Volume: 12

    Topics: Asian People; Base Sequence; Cataract; Child; Chromosome Mapping; Chromosomes, Human, Pair 21; Corne

2006
FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
    Molecular vision, 2007, Jan-26, Volume: 13

    Topics: Asian People; Blepharophimosis; Blepharoptosis; Cysteine; Cytosine; Eye Abnormalities; Eyelids; Fork

2007
Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
    Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology, 2008, Volume: 37, Issue:8

    Topics: Adolescent; Cephalometry; Chromosomes, Human, Pair 13; Codon; Cranial Fossa, Posterior; Craniofacial

2008