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5p13.1 GeneReviews Google OMIM Orphanet PubMed Who named it? Wikipedia [CDLS3] Cornelia de Lange syndrome *Gene map locus 5p13.1 Brachmann-de Lange syndrome CDLS Typus degenerativus Amstelodamensis [Clinical features: characteristic facies; growth retardation; mental retardation; upper limb anomalies] [Inheritance: autosomal dominant, isolated cases] |
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A case of Cornelia de Lange syndrome from Sudan |
A case of Cornelia de Lange syndrome from Sudan |
Cornelia De Lange Syndrome |
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Cornelia De Lange Syndrome |
Cornelia De Lange Syndrome |
de Lange Syndrome |
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eMedicine |
eMedicine |
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de Lange Syndrome |
de Lange Syndrome |
de Lange Syndrome |
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de Lange Syndrome |
de Lange Syndrome |
de Lange Syndrome |
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Edited by Aldo Campana,
March 14, 2010
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