Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome: Noncoding RAI1 deletion causes Smith-Magenis syndrome: U. Hamiel et al.
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| Title: | Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome: Noncoding RAI1 deletion causes Smith-Magenis syndrome: U. Hamiel et al. |
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| Authors: | Hamiel, Uri1,2 (AUTHOR) urihamiel@gmail.com, Kurolap, Alina1 (AUTHOR) alinak@tlvmc.gov.il, Chai Gadot, Chofit1 (AUTHOR) hofitg@tlvmc.gov.il, Mory, Adi1 (AUTHOR) adimory@tlvmc.gov.il, Bar Shira, Anat1 (AUTHOR) anatbn@tlvmc.gov.il, Baris Feldman, Hagit1,2 (AUTHOR) hagitbf@tlvmc.gov.il, Marom, Daphna1,2 (AUTHOR) daphnam@tlvmc.gov.il |
| Source: | Journal of Genetics. Jun2025, Vol. 104 Issue 1, p1-5. 5p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 184537483 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome: Noncoding RAI1 deletion causes Smith-Magenis syndrome: U. Hamiel et al. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Hamiel%2C+Uri%22">Hamiel, Uri</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> urihamiel@gmail.com</i><br /><searchLink fieldCode="AR" term="%22Kurolap%2C+Alina%22">Kurolap, Alina</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> alinak@tlvmc.gov.il</i><br /><searchLink fieldCode="AR" term="%22Chai+Gadot%2C+Chofit%22">Chai Gadot, Chofit</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> hofitg@tlvmc.gov.il</i><br /><searchLink fieldCode="AR" term="%22Mory%2C+Adi%22">Mory, Adi</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> adimory@tlvmc.gov.il</i><br /><searchLink fieldCode="AR" term="%22Bar+Shira%2C+Anat%22">Bar Shira, Anat</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> anatbn@tlvmc.gov.il</i><br /><searchLink fieldCode="AR" term="%22Baris+Feldman%2C+Hagit%22">Baris Feldman, Hagit</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> hagitbf@tlvmc.gov.il</i><br /><searchLink fieldCode="AR" term="%22Marom%2C+Daphna%22">Marom, Daphna</searchLink><relatesTo>1,2</relatesTo> (AUTHOR)<i> daphnam@tlvmc.gov.il</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Genetics%22">Journal of Genetics</searchLink>. Jun2025, Vol. 104 Issue 1, p1-5. 5p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=184537483 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1007/s12041-025-01497-x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1 Titles: – TitleFull: Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome: Noncoding RAI1 deletion causes Smith-Magenis syndrome: U. Hamiel et al. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Hamiel, Uri – PersonEntity: Name: NameFull: Kurolap, Alina – PersonEntity: Name: NameFull: Chai Gadot, Chofit – PersonEntity: Name: NameFull: Mory, Adi – PersonEntity: Name: NameFull: Bar Shira, Anat – PersonEntity: Name: NameFull: Baris Feldman, Hagit – PersonEntity: Name: NameFull: Marom, Daphna IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 06 Text: Jun2025 Type: published Y: 2025 Identifiers: – Type: issn-print Value: 00221333 Numbering: – Type: volume Value: 104 – Type: issue Value: 1 Titles: – TitleFull: Journal of Genetics Type: main |
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