Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.
Saved in:
| Title: | Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. |
|---|---|
| Authors: | Lamb NE; Department of Genetics, Emory University School of Medicine, Atlanta, GA, USA., Feingold E, Savage A, Avramopoulos D, Freeman S, Gu Y, Hallberg A, Hersey J, Karadima G, Pettay D, Saker D, Shen J, Taft L, Mikkelsen M, Petersen MB, Hassold T, Sherman SL |
| Source: | Human molecular genetics [Hum Mol Genet] 1997 Sep; Vol. 6 (9), pp. 1391-9. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. |
| Journal Info: | Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Print ISSN: 0964-6906 (Print) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 9285774 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Lamb+NE%22">Lamb NE</searchLink>; Department of Genetics, Emory University School of Medicine, Atlanta, GA, USA.<br /><searchLink fieldCode="AU" term="%22Feingold+E%22">Feingold E</searchLink><br /><searchLink fieldCode="AU" term="%22Savage+A%22">Savage A</searchLink><br /><searchLink fieldCode="AU" term="%22Avramopoulos+D%22">Avramopoulos D</searchLink><br /><searchLink fieldCode="AU" term="%22Freeman+S%22">Freeman S</searchLink><br /><searchLink fieldCode="AU" term="%22Gu+Y%22">Gu Y</searchLink><br /><searchLink fieldCode="AU" term="%22Hallberg+A%22">Hallberg A</searchLink><br /><searchLink fieldCode="AU" term="%22Hersey+J%22">Hersey J</searchLink><br /><searchLink fieldCode="AU" term="%22Karadima+G%22">Karadima G</searchLink><br /><searchLink fieldCode="AU" term="%22Pettay+D%22">Pettay D</searchLink><br /><searchLink fieldCode="AU" term="%22Saker+D%22">Saker D</searchLink><br /><searchLink fieldCode="AU" term="%22Shen+J%22">Shen J</searchLink><br /><searchLink fieldCode="AU" term="%22Taft+L%22">Taft L</searchLink><br /><searchLink fieldCode="AU" term="%22Mikkelsen+M%22">Mikkelsen M</searchLink><br /><searchLink fieldCode="AU" term="%22Petersen+MB%22">Petersen MB</searchLink><br /><searchLink fieldCode="AU" term="%22Hassold+T%22">Hassold T</searchLink><br /><searchLink fieldCode="AU" term="%22Sherman+SL%22">Sherman SL</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 1997 Sep; Vol. 6 (9), pp. 1391-9. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>0964-6906 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=9285774 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1093/hmg/6.9.1391 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 1391 Titles: – TitleFull: Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Lamb NE – PersonEntity: Name: NameFull: Feingold E – PersonEntity: Name: NameFull: Savage A – PersonEntity: Name: NameFull: Avramopoulos D – PersonEntity: Name: NameFull: Freeman S – PersonEntity: Name: NameFull: Gu Y – PersonEntity: Name: NameFull: Hallberg A – PersonEntity: Name: NameFull: Hersey J – PersonEntity: Name: NameFull: Karadima G – PersonEntity: Name: NameFull: Pettay D – PersonEntity: Name: NameFull: Saker D – PersonEntity: Name: NameFull: Shen J – PersonEntity: Name: NameFull: Taft L – PersonEntity: Name: NameFull: Mikkelsen M – PersonEntity: Name: NameFull: Petersen MB – PersonEntity: Name: NameFull: Hassold T – PersonEntity: Name: NameFull: Sherman SL IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 09 Text: 1997 Sep Type: published Y: 1997 Identifiers: – Type: issn-print Value: 0964-6906 Numbering: – Type: volume Value: 6 – Type: issue Value: 9 Titles: – TitleFull: Human molecular genetics Type: main |
| ResultId | 1 |