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11 Treffer
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Gender, genotype, and phenotype differences in Smith–Magenis syndrome: a meta-analysis of 105 cases.In: Clinical Genetics, Jg. 71 (2007-06-01), Heft 6, S. 540-550Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 72 (2007-09-01), Heft 3, S. 167-174Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 55 (1999-03-01), Heft 3, S. 173-181Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 75 (2009-03-01), Heft 3, S. 209-219Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 72 (2007-10-01), Heft 4, S. 271-287Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 60 (2001-08-01), Heft 2, S. 151-154Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 83 (2013-06-01), Heft 6, S. 560-564Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 79 (2011-03-01), Heft 3, S. 225-235Online academicJournalZugriff:
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A novel nonsense mutation in CUL4B gene in three brothers with X-linked mental retardation syndrome.In: Clinical Genetics, Jg. 77 (2010-02-01), Heft 2, S. 141-144Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 72 (2007-12-01), Heft 6, S. 593-598Online academicJournalZugriff:
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In: Clinical Genetics, Jg. 61 (2002-02-01), Heft 2, S. 139-145Online academicJournalZugriff: