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Shohat type-spondyloepimetaphyseal dysplasia: Further phenotypic delineation.

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Title: Shohat type-spondyloepimetaphyseal dysplasia: Further phenotypic delineation.
Authors: Otaify GA; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman. Electronic address: ghadaotaify@yahoo.com., Al Baluki W; Department of Surgery, Division of Orthopedic Surgery, College of Medicine and Health Sciences, Sultan Qaboos University, Sultan Qaboos University Hospital, Muscat, Oman., Al-Rashdi S; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman., Al-Maawali A; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
Source: European journal of medical genetics [Eur J Med Genet] 2022 Dec; Vol. 65 (12), pp. 104640. Date of Electronic Publication: 2022 Oct 13.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Shohat type-spondyloepimetaphyseal dysplasia: Further phenotypic delineation.
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  Data: <searchLink fieldCode="AU" term="%22Otaify+GA%22">Otaify GA</searchLink>; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman. Electronic address: ghadaotaify@yahoo.com.<br /><searchLink fieldCode="AU" term="%22Al+Baluki+W%22">Al Baluki W</searchLink>; Department of Surgery, Division of Orthopedic Surgery, College of Medicine and Health Sciences, Sultan Qaboos University, Sultan Qaboos University Hospital, Muscat, Oman.<br /><searchLink fieldCode="AU" term="%22Al-Rashdi+S%22">Al-Rashdi S</searchLink>; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman.<br /><searchLink fieldCode="AU" term="%22Al-Maawali+A%22">Al-Maawali A</searchLink>; Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman; Genetic and Developmental Medicine Clinic, Sultan Qaboos University Hospital, Muscat, Oman.
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  Data: <searchLink fieldCode="JN" term="%22101247089%22">European journal of medical genetics</searchLink> [Eur J Med Genet] 2022 Dec; Vol. 65 (12), pp. 104640. <i>Date of Electronic Publication: </i>2022 Oct 13.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier%22">Elsevier </searchLink><i>Country of Publication: </i>Netherlands <i>NLM ID: </i>101247089 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1878-0849 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2217697212%22">17697212 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Med Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1016/j.ejmg.2022.104640
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        Text: English
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              Text: 2022 Dec
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