2-propanol has been researched along with Labhart-Willi Syndrome in 8 studies
2-Propanol: An isomer of 1-PROPANOL. It is a colorless liquid having disinfectant properties. It is used in the manufacture of acetone and its derivatives and as a solvent. Topically, it is used as an antiseptic.
propan-2-ol : A secondary alcohol that is propane in which one of the hydrogens attached to the central carbon is substituted by a hydroxy group.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 8 (100.00) | 18.7374 |
1990's | 0 (0.00) | 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 |
---|---|
Gorlin, RJ | 1 |
de Grouchy, J | 2 |
Yunis, JJ | 1 |
Lewandowski, RC | 1 |
Hittner, HM | 1 |
King, RA | 1 |
Riccardi, VM | 1 |
Ledbetter, DH | 1 |
Borda, RP | 1 |
Ferrell, RE | 1 |
Kretzer, FL | 1 |
Schinzel, A | 1 |
Schmickel, RD | 1 |
Futterweit, W | 1 |
Ritch, R | 1 |
Teekhasaenee, C | 1 |
Nelson, ES | 1 |
Turleau, C | 1 |
5 reviews available for 2-propanol and Labhart-Willi Syndrome
Article | Year |
---|---|
Recent advances in cytogenetics.
Topics: Chromosome Banding; Chromosome Deletion; Chromosome Fragility; Cytogenetics; DiGeorge Syndrome; Flow | 1983 |
High-resolution cytogenetics.
Topics: Adolescent; Chromosome Aberrations; Chromosome Banding; Chromosome Deletion; Chromosomes, Human, 13- | 1983 |
[Newly discovered structural chromosome aberrations in long familial syndromes, associations and sequences. Prader-Willi syndrome, Miller-Dieker syndrome, Giedion-Langer syndrome, Aniridia-Wilms' tumor association, DiGeorge sequence, Wiedemann-Beckwith sy
Topics: Abnormalities, Multiple; Brain; Child; Chromosome Aberrations; Chromosome Disorders; DiGeorge Syndro | 1988 |
Contiguous gene syndromes: a component of recognizable syndromes.
Topics: Beckwith-Wiedemann Syndrome; Child; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping | 1986 |
Microcytogenetics 1984.
Topics: Beckwith-Wiedemann Syndrome; Brain; Chromosome Aberrations; Cytogenetics; DiGeorge Syndrome; Exostos | 1986 |
3 other studies available for 2-propanol and Labhart-Willi Syndrome
Article | Year |
---|---|
Toward clinical microcytogenetics: the aniridia and the retinoblastoma stories.
Topics: Abnormalities, Multiple; Chromosome Deletion; Chromosomes, Human, 13-15; Eye Neoplasms; Female; Huma | 1982 |
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndrome.
Topics: Adolescent; Adult; Child; Child, Preschool; Female; Hair; Humans; Iris; Male; Melanocytes; Monopheno | 1982 |
Coexistence of Prader-Willi syndrome, congenital ectropion uveae with glaucoma, and factor XI deficiency.
Topics: Adolescent; Clomiphene; Factor XI Deficiency; Follicle Stimulating Hormone; Glaucoma; Gonadotropin-R | 1986 |