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Patient Education | SingHealth Duke-NUS Genomic Medicine Centre
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Singapore Rare Disease Models and Mechanisms (RDMM) Network
Page Content
22q11.2 Deletion Syndrome
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Achondroplasia
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Citrin Deficiency
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Cowden Syndrome
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Genetic Testing
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Hereditary Paraganglioma-Phaeochromocytoma Syndrome
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Heritable Retinoblastoma
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Inherited Bone Marrow Failure Syndrome
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Inherited Retinal Diseases
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Klinefelter Syndrome
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Li-Fraumeni Syndrome
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Lynch Syndrome
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Marfan Syndrome
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Medium-Chain Acyl-CoA Dehydrogenase Deficiency
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Multiple Endocrine Neoplasia Type 1 (MEN1)
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Multiple Endocrine Neoplasia Type 2 (MEN2)
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Mitochondrial Diseases
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Neurofibromatosis Type 1
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Triple X Syndrome
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Turner Syndrome
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Von Hippel-Lindau Syndrome
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5/3/2023 8:45 AM
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