Congenital Duplication of the Palm Syndrome: Gene Analysis and the Molecular Basis of its Clinical Features - M. M. AL-QATTAN, M. AL-BALWI, W. EYAID, I. AL-ABDULKARIM, S. AL-TURKI, 2009
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Cornelia-de Lange syndrome in an Egyptian infant with unusual bone deformities - ScienceDirect
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The characteristic craniofacial features of Cornelia de Lange syndrome. | Download Scientific Diagram
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Cornelia de Lange Syndrome: A Variable Disorder of Cohesin Pathology | SpringerLink
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Cornelia De-Lange Syndrome: A Case Report | Semantic Scholar
TenderTouch Paediatric Rehab - What is CORNELIA DE LANGE SYNDROME Cornelia de Lange syndrome (CDLS), is a genetic disorder that causes a very distinct facial appearance that is present from birth. Infants
![Figure 2. [Hands of a woman age...]. - GeneReviews® - NCBI Bookshelf](https://www.ncbi.nlm.nih.gov/books/NBK425926/bin/tps-Image002.jpg "Figure 2. [Hands of a woman age...]. - GeneReviews® - NCBI Bookshelf")
Figure 2. [Hands of a woman age...]. - GeneReviews® - NCBI Bookshelf
Rare form of autosomal dominant familial Cornelia de Lange syndrome due to a novel duplication in SMC3 - Infante - 2017 - Clinical Case Reports - Wiley Online Library
Characteristic features of Cornelia de Lange syndrome. (A) Hirsutism.... | Download Scientific Diagram
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Cornelia de Lange syndrome - Wikipedia
