Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency.
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| Title: | Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. |
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| Authors: | Williams A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA., Divin K; Texas Children's Hospital, Houston, Texas, USA., Burrage LC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA., Craigen WJ; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA., Scaglia F; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Joint BCM-CUHK Center of Medical Genetics, Prince of Wales Hospital, Hong Kong SAR, China.; Baylor Genetics, Houston, Texas, USA., Soler-Alfonso C; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA., Sutton VR; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Baylor Genetics, Houston, Texas, USA., Glinton KE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA., Marom R; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2026 Apr 05. Date of Electronic Publication: 2026 Apr 05. |
| Publication Type: | Journal Article |
| 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 | Text: Availability: 0 |
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| Header | DbId: mdl DbLabel: MEDLINE Ultimate An: 41937280 AccessLevel: 2 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AU" term="%22Williams+A%22">Williams A</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Divin+K%22">Divin K</searchLink>; Texas Children's Hospital, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Burrage+LC%22">Burrage LC</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Craigen+WJ%22">Craigen WJ</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Scaglia+F%22">Scaglia F</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Joint BCM-CUHK Center of Medical Genetics, Prince of Wales Hospital, Hong Kong SAR, China.; Baylor Genetics, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Soler-Alfonso+C%22">Soler-Alfonso C</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Sutton+VR%22">Sutton VR</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.; Baylor Genetics, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Glinton+KE%22">Glinton KE</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA.<br /><searchLink fieldCode="AU" term="%22Marom+R%22">Marom R</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.; Texas Children's Hospital, Houston, Texas, USA. – 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] 2026 Apr 05. <i>Date of Electronic Publication: </i>2026 Apr 05. – Name: TypePub Label: Publication Type Group: TypPub Data: Journal Article – 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 |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41937280 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1002/ajmg.a.70154 Languages: – Code: eng Text: English Titles: – TitleFull: Developmental and Phenotypic Outcomes in Mild Phenylalanine Hydroxylase Deficiency. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Williams A – PersonEntity: Name: NameFull: Divin K – PersonEntity: Name: NameFull: Burrage LC – PersonEntity: Name: NameFull: Craigen WJ – PersonEntity: Name: NameFull: Scaglia F – PersonEntity: Name: NameFull: Soler-Alfonso C – PersonEntity: Name: NameFull: Sutton VR – PersonEntity: Name: NameFull: Glinton KE – PersonEntity: Name: NameFull: Marom R IsPartOfRelationships: – BibEntity: Dates: – D: 05 M: 04 Text: 2026 Apr 05 Type: published Y: 2026 Identifiers: – Type: issn-electronic Value: 1552-4833 Titles: – TitleFull: American journal of medical genetics. Part A Type: main |
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