File:DiGeorge 2.jpg: Difference between revisions

Latest revision as of 22:13, 9 September 2011

An image showing a young Indian male who has some of the abnormal facial features associated with DiGeorge syndrome

Original Text: Figure 1 Non-mosaic 22q11.2 microdeletion case. (A) Front view of face is showing broad nose, square shaped tip of nose, small philtrum, hypertelorism, telecanthus, squint and low set ears. (B) FISH image is showing one signal, indicating hemizygous 22q11.2 microdeletion.

Reference:

Ashutosh Halder, Manish Jain, Isha Chaudhary, Madhulika Kabra Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India. BMC Med. Genet.: 2010, 11();101 PMID:20573211 | PMC2912258

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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Yi efo/eka'e gwa ebo wo le nyangagi wuncin ye kamina wunga tinya nan

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Orientation	Normal
Horizontal resolution	72 dpi
Vertical resolution	72 dpi

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-PMCID: PMC2912258
-Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India
-This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
+An image showing a young Indian male who has some of the abnormal facial features associated with DiGeorge syndrome
-Figure 1
+Original Text: Figure 1
 Non-mosaic 22q11.2 microdeletion case. (A) Front view of face is showing broad nose, square shaped tip of nose, small philtrum, hypertelorism, telecanthus, squint and low set ears. (B) FISH image is showing one signal, indicating hemizygous 22q11.2 microdeletion.
+Reference:
+Ashutosh Halder, Manish Jain, Isha Chaudhary, Madhulika Kabra Prevalence of 22q11.2 microdeletion in 146 patients with cardiac malformation in a referral hospital of North India. BMC Med. Genet.: 2010, 11();101 PMID:20573211 | PMC2912258
+This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.