Clinical heterogeneity of Kabuki syndrome in a cohort of Italian patients and review of the literature
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Investigation of genetic and phenotypic heterogeneity in 37
Frontiers Case report: A study on the de novo KMT2D variant of
Clinical heterogeneity of Kabuki syndrome in a cohort of Italian
Clinical heterogeneity of Kabuki syndrome in a cohort of Italian
Facial phenotype of 2 Kabuki-like (A:KS2; B:KS14) and 2 Kabuki
PDF) Russell-Silver Syndrome: A Case Report with Review of
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Unraveling molecular pathways shared by Kabuki and Kabuki‐like
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Mutation spectrum of MLL2 in a cohort of kabuki syndrome patients
Kabuki syndrome: international consensus diagnostic criteria
A restricted spectrum of missense KMT2D variants cause a multiple
Autoimmune haematological disorders in two Italian children with
Orthodontic Treatment of a Kabuki Syndrome Patient
Patients with Kabuki syndrome and ITP. A: Patient 1, age 11 years
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