Contiguous gene deletion of TBX5 and TBX3: report of another case.

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Title: Contiguous gene deletion of TBX5 and TBX3: report of another case.
Authors: Forzano F; Departments of Clinical Genetics.; Department of Clinical Genetics, 7th Floor Borough Wing Guy's Hospital, Guy's & St Thomas' NHS Foundation Trust, London., Foley PA; Departments of Clinical Genetics., Keane MR; Department of Paediatrics, King George Hospital, Ilford, UK., Brain CE; Endocrinology., Smith GD; Plastic Surgery., Yates RW; Paediatric Cardiology., Ellershaw D; NE Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust., Calder AD; Radiology., Scott RH; Departments of Clinical Genetics.; Genomics England, Queen Mary University of London.
Source: Clinical dysmorphology [Clin Dysmorphol] 2018 Jan; Vol. 27 (1), pp. 6-8.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9207893 Publication Model: Print Cited Medium: Internet ISSN: 1473-5717 (Electronic) Linking ISSN: 09628827 NLM ISO Abbreviation: Clin Dysmorphol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Contiguous gene deletion of TBX5 and TBX3: report of another case.
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  Data: <searchLink fieldCode="AU" term="%22Forzano+F%22">Forzano F</searchLink>; Departments of Clinical Genetics.; Department of Clinical Genetics, 7th Floor Borough Wing Guy's Hospital, Guy's & St Thomas' NHS Foundation Trust, London.<br /><searchLink fieldCode="AU" term="%22Foley+PA%22">Foley PA</searchLink>; Departments of Clinical Genetics.<br /><searchLink fieldCode="AU" term="%22Keane+MR%22">Keane MR</searchLink>; Department of Paediatrics, King George Hospital, Ilford, UK.<br /><searchLink fieldCode="AU" term="%22Brain+CE%22">Brain CE</searchLink>; Endocrinology.<br /><searchLink fieldCode="AU" term="%22Smith+GD%22">Smith GD</searchLink>; Plastic Surgery.<br /><searchLink fieldCode="AU" term="%22Yates+RW%22">Yates RW</searchLink>; Paediatric Cardiology.<br /><searchLink fieldCode="AU" term="%22Ellershaw+D%22">Ellershaw D</searchLink>; NE Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust.<br /><searchLink fieldCode="AU" term="%22Calder+AD%22">Calder AD</searchLink>; Radiology.<br /><searchLink fieldCode="AU" term="%22Scott+RH%22">Scott RH</searchLink>; Departments of Clinical Genetics.; Genomics England, Queen Mary University of London.
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  Data: <searchLink fieldCode="JN" term="%229207893%22">Clinical dysmorphology</searchLink> [Clin Dysmorphol] 2018 Jan; Vol. 27 (1), pp. 6-8.
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  Data: Case Reports; Journal Article
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Lippincott+Williams+%26+Wilkins%22">Lippincott Williams & Wilkins </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9207893 <i>Publication Model: </i>Print <i>Cited Medium: </i>Internet <i>ISSN: </i>1473-5717 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209628827%22">09628827 </searchLink><i>NLM ISO Abbreviation: </i>Clin Dysmorphol <i>Subsets: </i>MEDLINE
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        Value: 10.1097/MCD.0000000000000199
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        Text: English
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              Text: 2018 Jan
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              Y: 2018
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