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Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome.

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Title: Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome.
Authors: Castro MAA; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil., Dos Santos JHV; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil., Honjo RS; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil., Yamamoto GL; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil., Bertola DR; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil., Hurst AC; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA., Chorich LP; Section of Reproductive Endocrinology, Infertility, & Genetics, Medical College of Georgia, Augusta University, Augusta, Georgia, USA., Layman LC; Section of Reproductive Endocrinology, Infertility, & Genetics, Medical College of Georgia, Augusta University, Augusta, Georgia, USA., Kim CA; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil., Kim HG; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2021 Dec; Vol. 185 (12), pp. 3916-3923. Date of Electronic Publication: 2021 Aug 18.
Publication Type: Case Reports; Research Support, Non-U.S. Gov't; 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
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  Data: Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome.
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  Data: <searchLink fieldCode="AU" term="%22Castro+MAA%22">Castro MAA</searchLink>; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Dos+Santos+JHV%22">Dos Santos JHV</searchLink>; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Honjo+RS%22">Honjo RS</searchLink>; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Yamamoto+GL%22">Yamamoto GL</searchLink>; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Bertola+DR%22">Bertola DR</searchLink>; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Hurst+AC%22">Hurst AC</searchLink>; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.<br /><searchLink fieldCode="AU" term="%22Chorich+LP%22">Chorich LP</searchLink>; Section of Reproductive Endocrinology, Infertility, & Genetics, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.<br /><searchLink fieldCode="AU" term="%22Layman+LC%22">Layman LC</searchLink>; Section of Reproductive Endocrinology, Infertility, & Genetics, Medical College of Georgia, Augusta University, Augusta, Georgia, USA.<br /><searchLink fieldCode="AU" term="%22Kim+CA%22">Kim CA</searchLink>; Unidade de Genética do Instituto da Criança-Hospital das Clínicas HCFMUSP, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Kim+HG%22">Kim HG</searchLink>; Neurological Disorders Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University, Doha, Qatar.
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  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. 3916-3923. <i>Date of Electronic Publication: </i>2021 Aug 18.
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  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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              M: 12
              Text: 2021 Dec
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