Compounds > neuromedin-b

neuromedin-b and Prader-Willi-Syndrome

neuromedin-b has been researched along with Prader-Willi-Syndrome* in 1 studies

Other Studies

1 other study(ies) available for neuromedin-b and Prader-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