Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature

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作者： Klaassens, Merel ^[1] ; Morrogh, Deborah ^[2] ; Rosser, Elisabeth M. ^[3] ; Jaffer, Fatima ^[4] ; Vreeburg, Maaike ^[5] ; Bok, Levinus A. ^[6] ; Segboer, Tim ; van Belzen, Martine ; Quinlivan, Ros M. ; Kumar, Ajith ; Hurst, Jane A. ; Scott, Richard H.

作者单位： Maxima Med Ctr, Dept Paediat, Belhaven, Netherlands ^[1] Maastricht Univ, Med Ctr, Dept Paediat, NL-6200 MD Maastricht, Netherlands ^[2] Maastricht Univ, Med Ctr, Dept Clin Genet, NL-6200 MD Maastricht, Netherlands ^[3] Great Ormond St Hosp Sick Children, North East Thames Reg Genet Serv, London WC1N 3JH, England ^[4] Leiden Univ, Med Ctr, Dept Clin Genet, Leiden, Netherlands ^[5] Natl Hosp Neurol & Neurosurg, MRC, Ctr Neuromuscular Dis, London WC1N 3BG, England ^[6]

发布时间 2015-07-17

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European journal of human genetics

2015年23卷5期

610-615页

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Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature

European journal of human genetics

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European journal of human genetics

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Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature

European journal of human genetics

相似文献

European journal of human genetics

相关期刊

检索历史清除