Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant

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Title: Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant
Authors: Gupta N; Vanderbilt University Medical Center, Department of Pediatrics, Division of Pediatric Endocrinology and Diabetes, Tennessee, USA; Mayo Clinic, Department of Pediatric and Adolescent Medicine, Division of Endocrinology and Metabolism, Minnesota, USA, Gregory SW; Mayo Clinic Health System, Department of Pediatric and Adolescent Medicine, Minnesota, USA, Deyle DR; Mayo Clinic, Department of Medical Genetics, Minnesota, USA, Tebben PJ; Mayo Clinic, Department of Pediatric and Adolescent Medicine, Division of Endocrinology and Metabolism, Minnesota, USA; Mayo Clinic, Department of Medicine, Division of Endocrinology, Metabolism and Nutrition, Minnesota, USA
Source: Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2021 Jun 02; Vol. 13 (2), pp. 218-224. Date of Electronic Publication: 2020 Jun 10.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Galenos Yayınevi Country of Publication: Turkey NLM ID: 101519456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1308-5735 (Electronic) NLM ISO Abbreviation: J Clin Res Pediatr Endocrinol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: <searchLink fieldCode="AU" term="%22Gupta+N%22">Gupta N</searchLink>; Vanderbilt University Medical Center, Department of Pediatrics, Division of Pediatric Endocrinology and Diabetes, Tennessee, USA; Mayo Clinic, Department of Pediatric and Adolescent Medicine, Division of Endocrinology and Metabolism, Minnesota, USA<br /><searchLink fieldCode="AU" term="%22Gregory+SW%22">Gregory SW</searchLink>; Mayo Clinic Health System, Department of Pediatric and Adolescent Medicine, Minnesota, USA<br /><searchLink fieldCode="AU" term="%22Deyle+DR%22">Deyle DR</searchLink>; Mayo Clinic, Department of Medical Genetics, Minnesota, USA<br /><searchLink fieldCode="AU" term="%22Tebben+PJ%22">Tebben PJ</searchLink>; Mayo Clinic, Department of Pediatric and Adolescent Medicine, Division of Endocrinology and Metabolism, Minnesota, USA; Mayo Clinic, Department of Medicine, Division of Endocrinology, Metabolism and Nutrition, Minnesota, USA
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  Data: <searchLink fieldCode="JN" term="%22101519456%22">Journal of clinical research in pediatric endocrinology</searchLink> [J Clin Res Pediatr Endocrinol] 2021 Jun 02; Vol. 13 (2), pp. 218-224. <i>Date of Electronic Publication: </i>2020 Jun 10.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Galenos+Yayınevi%22">Galenos Yayınevi </searchLink><i>Country of Publication: </i>Turkey <i>NLM ID: </i>101519456 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1308-5735 (Electronic) <i>NLM ISO Abbreviation: </i>J Clin Res Pediatr Endocrinol <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=32519829
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        Value: 10.4274/jcrpe.galenos.2020.2020.0012
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      – Code: eng
        Text: English
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        StartPage: 218
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      – TitleFull: Three Patient Kindred with a Novel Phenotype of Osteogenesis Imperfecta due to a COL1A1 Variant
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            NameFull: Gupta N
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            NameFull: Gregory SW
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            NameFull: Deyle DR
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            NameFull: Tebben PJ
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            – D: 02
              M: 06
              Text: 2021 Jun 02
              Type: published
              Y: 2021
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