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A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype.

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Bibliographic Details
Title: A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype.
Authors: Banker, Deepa1 (AUTHOR), Mungala, Bhavdeep1 (AUTHOR), Parekh, Zankhana1 (AUTHOR), Ganatra, Shachi1 (AUTHOR), Maheshwari, Vimal1 (AUTHOR), Raj, Yashica1 (AUTHOR), Patel, Utsav1 (AUTHOR), Patel, Digant1 (AUTHOR), Chamar, Kishan1 (AUTHOR), Solanki, Vasu1 (AUTHOR)
Source: Case Reports in Pediatrics. 3/11/2023, p1-5. 5p.
Database: Academic Search Ultimate
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Description
ISSN:20906803
DOI:10.1155/2023/2275582