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X Demographics
Title |
Frequency of chromosome 22q11.2 deletion among newborns with non-syndromic congenital heart defects from western Mexico
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Published in |
Boletín Médico del Hospital Infantil de México, November 2022
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DOI | 10.24875/bmhim.22000078 |
Pubmed ID | |
Authors |
Gerardo E Fabián-Morales, Lucina Bobadilla-Morales, Christian Peña-Padilla, Rafael Nieto-García, Pascuala B Rivera-Ramírez, Alfredo Corona-Rivera, Aurea Márquez-Mora, Graciela Macías-Salcedo, Idalid Cuero-Quezada, Jorge R Corona-Rivera |
X Demographics
The data shown below were collected from the profile of 1 X user who shared this research output. Click here to find out more about how the information was compiled.
Geographical breakdown
Country | Count | As % |
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Unknown | 1 | 100% |
Demographic breakdown
Type | Count | As % |
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Scientists | 1 | 100% |