RAD51 -Related Fanconi Anemia: Expanding the Phenotypic Spectrum and Strong Association With VACTERL.
Saved in:
| Title: | RAD51 -Related Fanconi Anemia: Expanding the Phenotypic Spectrum and Strong Association With VACTERL. |
|---|---|
| Authors: | Altintas B; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA., Stacy A; Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA., Gettinger K; Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA., Wilson DB; Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA., Shinawi MS; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA. |
| Source: | Clinical genetics [Clin Genet] 2026 Mar; Vol. 109 (3), pp. 591-597. Date of Electronic Publication: 2025 Sep 28. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Munksgaard Country of Publication: Denmark NLM ID: 0253664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1399-0004 (Electronic) Linking ISSN: 00099163 NLM ISO Abbreviation: Clin Genet Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Text: Availability: 0 |
|---|---|
| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41017074 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: RAD51 -Related Fanconi Anemia: Expanding the Phenotypic Spectrum and Strong Association With VACTERL. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Altintas+B%22">Altintas B</searchLink>; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA.<br /><searchLink fieldCode="AU" term="%22Stacy+A%22">Stacy A</searchLink>; Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA.<br /><searchLink fieldCode="AU" term="%22Gettinger+K%22">Gettinger K</searchLink>; Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA.<br /><searchLink fieldCode="AU" term="%22Wilson+DB%22">Wilson DB</searchLink>; Division of Hematology and Oncology, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA.<br /><searchLink fieldCode="AU" term="%22Shinawi+MS%22">Shinawi MS</searchLink>; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, Saint Louis, Missouri, USA. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%220253664%22">Clinical genetics</searchLink> [Clin Genet] 2026 Mar; Vol. 109 (3), pp. 591-597. <i>Date of Electronic Publication: </i>2025 Sep 28. – Name: TypePub Label: Publication Type Group: TypPub Data: Case Reports; Journal Article – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Munksgaard%22">Munksgaard </searchLink><i>Country of Publication: </i>Denmark <i>NLM ID: </i>0253664 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1399-0004 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2200099163%22">00099163 </searchLink><i>NLM ISO Abbreviation: </i>Clin Genet <i>Subsets: </i>MEDLINE |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41017074 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/cge.70077 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 591 Titles: – TitleFull: RAD51 -Related Fanconi Anemia: Expanding the Phenotypic Spectrum and Strong Association With VACTERL. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Altintas B – PersonEntity: Name: NameFull: Stacy A – PersonEntity: Name: NameFull: Gettinger K – PersonEntity: Name: NameFull: Wilson DB – PersonEntity: Name: NameFull: Shinawi MS IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2026 Mar Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1399-0004 Numbering: – Type: volume Value: 109 – Type: issue Value: 3 Titles: – TitleFull: Clinical genetics Type: main |
| ResultId | 1 |