File:PMC4555966 tacg-8-189Fig1.png

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PMC4555966_tacg-8-189Fig1.png ‎(512 × 347 pixels, file size: 446 KB, MIME type: image/png)

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[Attribution-NonCommercial 3.0 Unported (CC BY-NC 3.0)

Summary

Author:Jordan VK, Zaveri HP, Scott DA,Department of Molecular Physiology and Biophysics, Baylor College of Medicine (Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4555966_tacg-8-189Fig1&query=1p36%20deletion%20syndrome&it=xg&req=4&npos=2 Description:f1-tacg-8-189: Facial features of a girl with a terminal 1p36 deletion (chr1:1–3,047,838; GRCh37/hg19).Notes: Photos were taken at (A) 1 year 8 months, (B) 2 years 3 months, (C) 4 years, (D) 7 years, (E) 7 years 11 months, and (F) 10 years 3 months of age. These photos demonstrate several facial features that are typical of children with terminal 1p36 deletions, including straight eyebrows, a wide nasal bridge, and a pointed chin.

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Date/TimeThumbnailDimensionsUserComment
current20:59, 28 September 2021Thumbnail for version as of 20:59, 28 September 2021512 × 347 (446 KB)Ozzie10aaaaAuthor:Jordan VK, Zaveri HP, Scott DA,Department of Molecular Physiology and Biophysics, Baylor College of Medicine (Openi/National Library of Medicine) Source:https://openi.nlm.nih.gov/detailedresult?img=PMC4555966_tacg-8-189Fig1&query=1p36%20deletion%20syndrome&it=xg&req=4&npos=2 Description:f1-tacg-8-189: Facial features of a girl with a terminal 1p36 deletion (chr1:1–3,047,838; GRCh37/hg19).Notes: Photos were taken at (A) 1 year 8 months, (B) 2 years 3 months, (C) 4 years, (D) 7 years, (E...

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