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Genetic Overlap between Holoprosencephaly and Kallmann Syndrome

Patients with Kallmann syndrome (KS; congenital hypogonadotropic hypogonadism and decreased/absent sense of smell), septo-optic dysplasia (SOD), or holoprosencephaly (HPE) reportedly have midline defects. In this study, we investigate a genetic overlap between KS, SOD, and HPE. Nineteen subjects (18...

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Bibliografski detalji
Glavni autori: Vaaralahti, K., Raivio, T., Koivu, R., Valanne, L., Laitinen, E.-M., Tommiska, J.
Format: Artigo
Jezik:Inglês
Izdano: S. Karger AG 2012
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3398826/
https://ncbi.nlm.nih.gov/pubmed/22855648
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000338706
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