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Updated: Feb 23, 2026

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Laser Capture Microdissection of Mouse Embryonic Cartilage and Bone for Gene Expression Analysis
Published on: December 18, 2019
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Severe phenotype of X-linked dominant chondrodysplasia punctata
Nadirah Damseh1, Karen Chong1,2, Christian Marshall1
1Division of Clinical and Metabolic Genetics The Hospital for Sick Children University of Toronto Toronto Ontario M5G 1X8 Canada.
Clinical Case Reports
|September 8, 2017
Abstract:
A prenatally ascertained case representing the more severe end of the X-linked dominant chondrodysplasia punctata (CDPX2).
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