نتائج البحث - Haneen Jabaly-Habib

A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay حسب Zufit Hexner-Erlichman, Boris Fichtman, Yoav Zehavi, Yoav Zehavi, Morad Khayat, Haneen Jabaly-Habib, Haneen Jabaly-Habib, Lee S. Izhaki-Tavor, Moshe Dessau, Orly Elpeleg, Ronen Spiegel, Ronen Spiegel

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