PDGFRB mutation causes autosomal-dominant Penttinen syndrome
10.1111/cge.12680
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sg-nus-scholar.10635-2350982024-04-17T08:36:34Z PDGFRB mutation causes autosomal-dominant Penttinen syndrome Aminkeng, F MEDICINE Science & Technology Life Sciences & Biomedicine Genetics & Heredity 10.1111/cge.12680 CLINICAL GENETICS 88 6 531-U7 2022-12-01T08:33:53Z 2022-12-01T08:33:53Z 2015-12-01 2022-11-30T18:48:26Z Article Aminkeng, F (2015-12-01). PDGFRB mutation causes autosomal-dominant Penttinen syndrome. CLINICAL GENETICS 88 (6) : 531-U7. ScholarBank@NUS Repository. https://doi.org/10.1111/cge.12680 0009-9163 1399-0004 https://scholarbank.nus.edu.sg/handle/10635/235098 en WILEY-BLACKWELL Elements |
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Science & Technology Life Sciences & Biomedicine Genetics & Heredity Aminkeng, F PDGFRB mutation causes autosomal-dominant Penttinen syndrome |
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10.1111/cge.12680 |
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MEDICINE |
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MEDICINE Aminkeng, F |
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Article |
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Aminkeng, F |
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Aminkeng, F |
title |
PDGFRB mutation causes autosomal-dominant Penttinen syndrome |
title_short |
PDGFRB mutation causes autosomal-dominant Penttinen syndrome |
title_full |
PDGFRB mutation causes autosomal-dominant Penttinen syndrome |
title_fullStr |
PDGFRB mutation causes autosomal-dominant Penttinen syndrome |
title_full_unstemmed |
PDGFRB mutation causes autosomal-dominant Penttinen syndrome |
title_sort |
pdgfrb mutation causes autosomal-dominant penttinen syndrome |
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WILEY-BLACKWELL |
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2022 |
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https://scholarbank.nus.edu.sg/handle/10635/235098 |
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