Search Results - "Ge, HongSong"
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A mutation in CCDC91, Homo sapiens coiled-coil domain containing 91 protein, cause autosomal-dominant acrokeratoelastoidosis
Published in European journal of human genetics : EJHG (01-06-2024)“…Acrokeratoelastoidosis (AKE) is a rare autosomal dominant hereditary skin disease characterized by small, round-oval, flat-topped keratotic papules on the…”
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Clinical and molecular characteristics of thirty NF1 variants in Chinese patients with neurofibromatosis type 1
Published in Molecular biology reports (01-08-2019)“…Neurofibromatosis type 1 (NF1) is a common autosomal dominant tumor-predisposition disorder that mainly impacts the nervous system and skin. Since the full…”
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Variations in RASA1 and EPHB4 in Chinese patients with capillary malformation-arteriovenous malformation
Published in Journal of dermatology (22-11-2024)“…Capillary malformation-arteriovenous malformation (CM-AVM) is a genetic condition predominantly attributed to variations in the RASA1 or EPHB4 genes. We…”
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A Real-Time Photo-Realistic Rendering Algorithm of Ocean Color Based on Bio-Optical Model
Published in Journal of Ocean University of China (01-12-2016)“…Abstract A real-time photo-realistic rendering algorithm of ocean color is introduced in the paper, which considers the impact of ocean bio-optical model. The…”
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