Clinical and genetic characteristics and prenatal diagnosis of patients presented GDD/ID with rare monogenic causes.
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| Title: | Clinical and genetic characteristics and prenatal diagnosis of patients presented GDD/ID with rare monogenic causes. |
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| Authors: | Lin, Liling1 (AUTHOR), Zhang, Ying1 (AUTHOR), Pan, Hong1 (AUTHOR), Wang, Jingmin2 (AUTHOR), Qi, Yu1 (AUTHOR), Ma, Yinan1 (AUTHOR) mayinan1014@163.com |
| Source: | Orphanet Journal of Rare Diseases. 11/11/2020, Vol. 15 Issue 1, pN.PAG-N.PAG. 1p. |
| Database: | Academic Search Ultimate |
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| Header | DbId: asn DbLabel: Academic Search Ultimate An: 146950474 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Clinical and genetic characteristics and prenatal diagnosis of patients presented GDD/ID with rare monogenic causes. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Lin%2C+Liling%22">Lin, Liling</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Zhang%2C+Ying%22">Zhang, Ying</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pan%2C+Hong%22">Pan, Hong</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Wang%2C+Jingmin%22">Wang, Jingmin</searchLink><relatesTo>2</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Qi%2C+Yu%22">Qi, Yu</searchLink><relatesTo>1</relatesTo> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ma%2C+Yinan%22">Ma, Yinan</searchLink><relatesTo>1</relatesTo> (AUTHOR)<i> mayinan1014@163.com</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Orphanet+Journal+of+Rare+Diseases%22">Orphanet Journal of Rare Diseases</searchLink>. 11/11/2020, Vol. 15 Issue 1, pN.PAG-N.PAG. 1p. |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=146950474 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1186/s13023-020-01599-y Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 1 StartPage: N.PAG Titles: – TitleFull: Clinical and genetic characteristics and prenatal diagnosis of patients presented GDD/ID with rare monogenic causes. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lin, Liling – PersonEntity: Name: NameFull: Zhang, Ying – PersonEntity: Name: NameFull: Pan, Hong – PersonEntity: Name: NameFull: Wang, Jingmin – PersonEntity: Name: NameFull: Qi, Yu – PersonEntity: Name: NameFull: Ma, Yinan IsPartOfRelationships: – BibEntity: Dates: – D: 11 M: 11 Text: 11/11/2020 Type: published Y: 2020 Identifiers: – Type: issn-print Value: 17501172 Numbering: – Type: volume Value: 15 – Type: issue Value: 1 Titles: – TitleFull: Orphanet Journal of Rare Diseases Type: main |
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