Menke-Hennekam syndrome; delineation of domain-specific subtypes with distinct clinical and DNA methylation profiles

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Publikováno v: In Human Genetics and Genomics Advances 18 July 2024 5(3)

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Neurogenic Defects Occur in LRIG2-Associated Urinary Bladder Disease

Autor: Grenier, Celine, Lopes, Filipa M., Cueto-González, Anna M., Rovira-Moreno, Eulàlia, Gander, Romy, Jarvis, Benjamin W., McCloskey, Karen D., Gurney, Alison M., Beaman, Glenda M., Newman, William G., Woolf, Adrian S., Roberts, Neil A.

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