Associated Papers
Pattern Recognition of Common Multiple Congenital Malformation Syndromes with Underlying Chromatinopathy.
Kaur A et al.
Journal of Pediatric Genetics, 2024
Clinical and molecular analysis of Guangxi patients with Kabuki syndrome and KMT2D mutations.
Yi S et al.
Heliyon, 2023
37810849 (PubMed )
Supplement: mmc4.xlsx › Variants_of_P_or_LP
Congenital heart defects in molecularly proven Kabuki syndrome patients.
Digilio MC et al.
American Journal of Medical Genetics. Part A, 2017
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