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Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience.

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Title: Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience.
Authors: Bilge, Serap1 (AUTHOR) sarabsmustafa@hotmail.com, Mert, Gülen Gül1 (AUTHOR), Hergüner, Özlem1 (AUTHOR), Özcanyüz, Duygu1 (AUTHOR), Bozdoğan, Sevcan Tuğ2 (AUTHOR), Kaya, Ömer3 (AUTHOR), Havalı, Cengiz4 (AUTHOR)
Source: Italian Journal of Pediatrics. 9/8/2022, Vol. 48 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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An: 158998412
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PubType: Academic Journal
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  Data: Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience.
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  Data: <searchLink fieldCode="AR" term="%22Bilge%2C+Serap%22">Bilge, Serap</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> sarabsmustafa@hotmail.com</i><br /><searchLink fieldCode="AR" term="%22Mert%2C+Gülen+Gül%22">Mert, Gülen Gül</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Hergüner%2C+Özlem%22">Hergüner, Özlem</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Özcanyüz%2C+Duygu%22">Özcanyüz, Duygu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Bozdoğan%2C+Sevcan+Tuğ%22">Bozdoğan, Sevcan Tuğ</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kaya%2C+Ömer%22">Kaya, Ömer</searchLink><relatesTo>3</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Havalı%2C+Cengiz%22">Havalı, Cengiz</searchLink><relatesTo>4</relatesTo> (AUTHOR)
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  Data: <searchLink fieldCode="JN" term="%22Italian+Journal+of+Pediatrics%22">Italian Journal of Pediatrics</searchLink>. 9/8/2022, Vol. 48 Issue 1, p1-8. 8p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=158998412
RecordInfo BibRecord:
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        Value: 10.1186/s13052-022-01349-9
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        Text: English
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      – TitleFull: Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience.
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            NameFull: Bilge, Serap
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            NameFull: Mert, Gülen Gül
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              M: 09
              Text: 9/8/2022
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              Y: 2022
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