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

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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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  Data: A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype.
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  Data: <searchLink fieldCode="AR" term="%22Banker%2C+Deepa%22">Banker, Deepa</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mungala%2C+Bhavdeep%22">Mungala, Bhavdeep</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Parekh%2C+Zankhana%22">Parekh, Zankhana</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ganatra%2C+Shachi%22">Ganatra, Shachi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Maheshwari%2C+Vimal%22">Maheshwari, Vimal</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Raj%2C+Yashica%22">Raj, Yashica</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Patel%2C+Utsav%22">Patel, Utsav</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Patel%2C+Digant%22">Patel, Digant</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Chamar%2C+Kishan%22">Chamar, Kishan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Solanki%2C+Vasu%22">Solanki, Vasu</searchLink><relatesTo>1</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Case+Reports+in+Pediatrics%22">Case Reports in Pediatrics</searchLink>. 3/11/2023, p1-5. 5p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=162418860
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      – Type: doi
        Value: 10.1155/2023/2275582
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      – Code: eng
        Text: English
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      – TitleFull: A Neonatal Patient Diagnosed with Chromosome 18p 11.1 Microdeletion Syndrome Presented with Trisomy 18Like Phenotype.
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            NameFull: Banker, Deepa
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            NameFull: Mungala, Bhavdeep
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            NameFull: Parekh, Zankhana
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            NameFull: Ganatra, Shachi
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            – D: 11
              M: 03
              Text: 3/11/2023
              Type: published
              Y: 2023
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            – TitleFull: Case Reports in Pediatrics
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