Expanding the KIF4A-associated phenotype.
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| Title: | Expanding the KIF4A-associated phenotype. |
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| Authors: | Kalantari S; Medical Genetics, Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.; Department of Clinical Research, University Hospital Basel, Basel, Switzerland., Carlston C; Division of Medical Genetics, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA., Alsaleh N; Division of Medical Genetics and Metabolic Medicine, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia., Abdel-Salam GMH; Department of Clinical Genetics, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt., Alkuraya F; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Kato M; Department of Pediatrics, Showa University School of Medicine, Shinagawa-ku, Japan., Matsumoto N; Department of Human Genetics, Yokohama City University, Graduate School of Medicine, Yokohama, Japan., Miyatake S; Department of Human Genetics, Yokohama City University, Graduate School of Medicine, Yokohama, Japan., Yamamoto T; Department of Pediatrics, Hirosaki University School of Medicine, Hirosaki, Japan., Fares-Taie L; INSERM UMR1163, Imagine - Institute of Genetic Diseases, Paris Descartes University, Paris, France., Rozet JM; INSERM UMR1163, Imagine - Institute of Genetic Diseases, Paris Descartes University, Paris, France., Chassaing N; Department of Medical Genetics, CHU Toulouse, Purpan Hospital, Toulouse, France., Vincent-Delorme C; Department of Clinical Genetics, CHU Lille, Lille, France., Kang-Bellin A; Centre for Prenatal Ultrasound, Basel, Switzerland., McWalter K; GeneDx, 207 Perry Parkway, Gaithersburg, Maryland, USA., Bupp C; Spectrum Health, Grand Rapids, Michigan, USA., Palen E; Autism & Developmental Medicine Institute, Danville, Pennsylvania, USA., Wagner MD; Autism & Developmental Medicine Institute, Danville, Pennsylvania, USA., Niceta M; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Cesario C; Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Milone R; Department of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Calambrone, Pisa, Italy., Kaplan J; Division of Genetics, Department of Pediatrics, Nemours/Alfred I. DuPont Hospital for Children, Wilmington, Delaware, USA., Wadman E; Division of Genetics, Department of Pediatrics, Nemours/Alfred I. DuPont Hospital for Children, Wilmington, Delaware, USA., Dobyns WB; Division of Genetics, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota, USA., Filges I; Medical Genetics, Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.; Department of Clinical Research, University Hospital Basel, Basel, Switzerland.; University of Basel, Basel, Switzerland. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2021 Dec; Vol. 185 (12), pp. 3728-3739. Date of Electronic Publication: 2021 Aug 03. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 34346154 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Expanding the KIF4A-associated phenotype. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Kalantari+S%22">Kalantari S</searchLink>; Medical Genetics, Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.; Department of Clinical Research, University Hospital Basel, Basel, Switzerland.<br /><searchLink fieldCode="AU" term="%22Carlston+C%22">Carlston C</searchLink>; Division of Medical Genetics, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.<br /><searchLink fieldCode="AU" term="%22Alsaleh+N%22">Alsaleh N</searchLink>; Division of Medical Genetics and Metabolic Medicine, Department of Pediatrics, Prince Sultan Military Medical City, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Abdel-Salam+GMH%22">Abdel-Salam GMH</searchLink>; Department of Clinical Genetics, Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt.<br /><searchLink fieldCode="AU" term="%22Alkuraya+F%22">Alkuraya F</searchLink>; Department of Translational Genomics, Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.<br /><searchLink fieldCode="AU" term="%22Kato+M%22">Kato M</searchLink>; Department of Pediatrics, Showa University School of Medicine, Shinagawa-ku, Japan.<br /><searchLink fieldCode="AU" term="%22Matsumoto+N%22">Matsumoto N</searchLink>; Department of Human Genetics, Yokohama City University, Graduate School of Medicine, Yokohama, Japan.<br /><searchLink fieldCode="AU" term="%22Miyatake+S%22">Miyatake S</searchLink>; Department of Human Genetics, Yokohama City University, Graduate School of Medicine, Yokohama, Japan.<br /><searchLink fieldCode="AU" term="%22Yamamoto+T%22">Yamamoto T</searchLink>; Department of Pediatrics, Hirosaki University School of Medicine, Hirosaki, Japan.<br /><searchLink fieldCode="AU" term="%22Fares-Taie+L%22">Fares-Taie L</searchLink>; INSERM UMR1163, Imagine - Institute of Genetic Diseases, Paris Descartes University, Paris, France.<br /><searchLink fieldCode="AU" term="%22Rozet+JM%22">Rozet JM</searchLink>; INSERM UMR1163, Imagine - Institute of Genetic Diseases, Paris Descartes University, Paris, France.<br /><searchLink fieldCode="AU" term="%22Chassaing+N%22">Chassaing N</searchLink>; Department of Medical Genetics, CHU Toulouse, Purpan Hospital, Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Vincent-Delorme+C%22">Vincent-Delorme C</searchLink>; Department of Clinical Genetics, CHU Lille, Lille, France.<br /><searchLink fieldCode="AU" term="%22Kang-Bellin+A%22">Kang-Bellin A</searchLink>; Centre for Prenatal Ultrasound, Basel, Switzerland.<br /><searchLink fieldCode="AU" term="%22McWalter+K%22">McWalter K</searchLink>; GeneDx, 207 Perry Parkway, Gaithersburg, Maryland, USA.<br /><searchLink fieldCode="AU" term="%22Bupp+C%22">Bupp C</searchLink>; Spectrum Health, Grand Rapids, Michigan, USA.<br /><searchLink fieldCode="AU" term="%22Palen+E%22">Palen E</searchLink>; Autism & Developmental Medicine Institute, Danville, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Wagner+MD%22">Wagner MD</searchLink>; Autism & Developmental Medicine Institute, Danville, Pennsylvania, USA.<br /><searchLink fieldCode="AU" term="%22Niceta+M%22">Niceta M</searchLink>; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Cesario+C%22">Cesario C</searchLink>; Laboratory of Medical Genetics, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.<br /><searchLink fieldCode="AU" term="%22Milone+R%22">Milone R</searchLink>; Department of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Calambrone, Pisa, Italy.<br /><searchLink fieldCode="AU" term="%22Kaplan+J%22">Kaplan J</searchLink>; Division of Genetics, Department of Pediatrics, Nemours/Alfred I. DuPont Hospital for Children, Wilmington, Delaware, USA.<br /><searchLink fieldCode="AU" term="%22Wadman+E%22">Wadman E</searchLink>; Division of Genetics, Department of Pediatrics, Nemours/Alfred I. DuPont Hospital for Children, Wilmington, Delaware, USA.<br /><searchLink fieldCode="AU" term="%22Dobyns+WB%22">Dobyns WB</searchLink>; Division of Genetics, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota, USA.<br /><searchLink fieldCode="AU" term="%22Filges+I%22">Filges I</searchLink>; Medical Genetics, Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.; Department of Clinical Research, University Hospital Basel, Basel, Switzerland.; University of Basel, Basel, Switzerland. – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2021 Dec; Vol. 185 (12), pp. 3728-3739. <i>Date of Electronic Publication: </i>2021 Aug 03. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article; Research Support, Non-U.S. Gov't – Name: TitleSource Label: Journal Info Group: Src Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1552-4833 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.62443 Languages: – Code: eng Text: English PhysicalDescription: Pagination: StartPage: 3728 Titles: – TitleFull: Expanding the KIF4A-associated phenotype. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Kalantari S – PersonEntity: Name: NameFull: Carlston C – PersonEntity: Name: NameFull: Alsaleh N – PersonEntity: Name: NameFull: Abdel-Salam GMH – PersonEntity: Name: NameFull: Alkuraya F – PersonEntity: Name: NameFull: Kato M – PersonEntity: Name: NameFull: Matsumoto N – PersonEntity: Name: NameFull: Miyatake S – PersonEntity: Name: NameFull: Yamamoto T – PersonEntity: Name: NameFull: Fares-Taie L – PersonEntity: Name: NameFull: Rozet JM – PersonEntity: Name: NameFull: Chassaing N – PersonEntity: Name: NameFull: Vincent-Delorme C – PersonEntity: Name: NameFull: Kang-Bellin A – PersonEntity: Name: NameFull: McWalter K – PersonEntity: Name: NameFull: Bupp C – PersonEntity: Name: NameFull: Palen E – PersonEntity: Name: NameFull: Wagner MD – PersonEntity: Name: NameFull: Niceta M – PersonEntity: Name: NameFull: Cesario C – PersonEntity: Name: NameFull: Milone R – PersonEntity: Name: NameFull: Kaplan J – PersonEntity: Name: NameFull: Wadman E – PersonEntity: Name: NameFull: Dobyns WB – PersonEntity: Name: NameFull: Filges I IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 12 Text: 2021 Dec Type: published Y: 2021 Identifiers: – Type: issn-electronic Value: 1552-4833 Numbering: – Type: volume Value: 185 – Type: issue Value: 12 Titles: – TitleFull: American journal of medical genetics. Part A Type: main |
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