RT @reinmd77: 35yo♂️📈deform finger camptodactyly ESR/CRP⬆️ 🔑deaf FHx++ 🧬SLC29A3 mutat ◾H syndrome https://t.co/t4GLgAp2jL Full Phenotype…
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35yo♂️📈deform finger camptodactyly ESR/CRP⬆️ 🔑deaf FHx++ 🧬SLC29A3 mutat ◾H syndrome https://t.co/t4GLgAp2jL Full Phenotype Hyperpigment Hypertrich Hepatosplen⬆️ Hear⬇️ Heart anoma Hypogon height⬇️ HyperglycDM Hallux/flex contrac https://t.co/oCDgiBlNKi
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A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature. https://t.co/x621BpzMcZ
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A novel homozygous frame-shift mutation in the SLC29A3 gene: a new case report and review of literature. https://t.co/dbhWRoaTSa