Associated Papers
Exome Sequencing Reveals the Genetic Architecture of Non-syndromic Orofacial Clefts and Identifies BOC as a Novel Causal Gene.
He Q et al.
Advanced Science (weinheim, Baden-wurttemberg, Germany), 2025
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Supplement: ADVS-12-e12073-s006.xlsx › Sheet1
Disorders of Sex Development in Individuals Harbouring MAMLD1 Variants: WES and Interactome Evidence of Oligogenic Inheritance.
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Frontiers in Endocrinology, 2020
Wolf-Hirschhorn (4P-) syndrome in adults.
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Genetic Counseling (geneva, Switzerland), 2001
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