Compounds > neurokinin b
Page last updated: 2024-08-23

neurokinin b and Labhart-Willi Syndrome

neurokinin b has been researched along with Labhart-Willi Syndrome in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gregory, CA; Schwartz, JS1

Other Studies

1 other study(ies) available for neurokinin b and Labhart-Willi Syndrome

ArticleYear
The cDNA of the human neuromedin B gene (NMB) mapped to 15q11-qter recognizes an XbaI RFLP.
    Nucleic acids research, 1991, Mar-11, Volume: 19, Issue:5

    Topics: Chromosome Mapping; Chromosomes, Human, Pair 15; Deoxyribonucleases, Type II Site-Specific; DNA Probes; Humans; Neurokinin B; Polymorphism, Restriction Fragment Length; Prader-Willi Syndrome

1991