A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes.
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| Title: | A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes. |
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| Authors: | Nardello, Rosaria1 (AUTHOR) rosaria.nardello@unipa.it, Antona, Vincenzo1 (AUTHOR), Mangano, Giuseppe Donato1 (AUTHOR), Salpietro, Vincenzo2 (AUTHOR), Mangano, Salvatore1 (AUTHOR), Fontana, Antonina1 (AUTHOR) |
| Source: | BMC Medical Genomics. 4/8/2021, Vol. 14 Issue 1, p1-5. 5p. |
| Database: | Academic Search Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 149713946 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=149713946 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s12920-021-00934-x Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 5 StartPage: 1 Titles: – TitleFull: A paradigmatic autistic phenotype associated with loss of PCDH11Y and NLGN4Y genes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Nardello, Rosaria – PersonEntity: Name: NameFull: Antona, Vincenzo – PersonEntity: Name: NameFull: Mangano, Giuseppe Donato – PersonEntity: Name: NameFull: Salpietro, Vincenzo – PersonEntity: Name: NameFull: Mangano, Salvatore – PersonEntity: Name: NameFull: Fontana, Antonina IsPartOfRelationships: – BibEntity: Dates: – D: 08 M: 04 Text: 4/8/2021 Type: published Y: 2021 Identifiers: – Type: issn-print Value: 17558794 Numbering: – Type: volume Value: 14 – Type: issue Value: 1 Titles: – TitleFull: BMC Medical Genomics Type: main |
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