Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay. (Q47880709)
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scientific article published in May 1998
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English | Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay. |
scientific article published in May 1998 |
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Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and developmental delay. (English)
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Upadhyaya M
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Maynard J
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Osborn M
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Hartog C
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Mudd S
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Penttinen M
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Cordeiro I
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Ponder M
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Ponder BA
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Krawczak M
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1 May 1998
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102
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5
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591-597
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