15q11.2 microdeletion (BP1–BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: A series of 52 patients

Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent‐Delorme, Sonia Bouquillon, Odile Boute, Muriel Holder‐Espinasse, Bruno Delobel, Bénédicte Duban, Louis Vallée,

European Journal of Medical Genetics · 2015 · 120 citations · 44 references

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