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Springer Publishing Company

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Symptomatic anal anomalies in chromosome 22q11 deletion syndrome: a report of three patients

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Frequency of thrombocytopenia and large platelets correlates neither with conotruncal cardiac anomalies nor immunological features in the chromosome 22q11.2 deletion syndrome

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Terminal Deletion 2q37.3 in a Patient with Klippel-Trenaunay-Weber Syndrome

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Fulminant autoimmune hepatitis in a girl with 22q13 deletion syndrome: a previously unreported association

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