File:12881 2017 486 Fig1 HTML (1).jpg

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MECP2 duplication syndrome

Summary[edit]

Description
English: The Chinese family with MECP2 duplication syndrome. a Pedigree of the Chinese family. b Facial features of the affected male patients (a. III:16 at 11 years and 2 months old. b. III:6 at 24 years old. c. IV:2 at 2 years and 10 months old. d. IV:1 at 14 years and 8 months old). They show consistent and typical facial features of MECP2 duplication syndrome, such as midface hypoplasia, long face, down-slanting palpebral fissures, epicanthus, small mouth, jaw protrusion, low-set ears, and large ear lobe and crease
Date
Source https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688748/
Author Li X, Xie H, Chen Q, Yu X, Yi Z, Li E, Zhang T, Wang J, Zhong J, Chen X.

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current23:31, 3 March 2024Thumbnail for version as of 23:31, 3 March 2024347 × 279 (28 KB)Ozzie10aaaa (talk | contribs)Uploaded a work by Li X, Xie H, Chen Q, Yu X, Yi Z, Li E, Zhang T, Wang J, Zhong J, Chen X. from https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688748/ with UploadWizard

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