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Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature.
Shelby, Elena-Silvia; Morris, Michael; Padure, Liliana; Mirea, Andrada; Cocoș, Relu; Caramizaru, Alexandru; Șerban-Sosoi, Simona; Pîrvu, Andrei; Streața, Ioana.
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  • Shelby ES; National University Center for Children's Neurorehabilitation "Dr. Nicolae Robanescu", 44 Dumitru Minca Street, District 4, 041408 Bucharest, Romania.
  • Morris M; Department of Genetics, SYNLAB Switzerland, Chemin d'Entre-Bois 21, 1018 Lausanne, Switzerland.
  • Padure L; National University Center for Children's Neurorehabilitation "Dr. Nicolae Robanescu", 44 Dumitru Minca Street, District 4, 041408 Bucharest, Romania.
  • Mirea A; Faculty of Midwifery and Nursing, University of Medicine and Pharmacy "Carol Davila", 8 Eroilor Sanitari Boulevard, 050474 Bucharest, Romania.
  • Cocoș R; National University Center for Children's Neurorehabilitation "Dr. Nicolae Robanescu", 44 Dumitru Minca Street, District 4, 041408 Bucharest, Romania.
  • Caramizaru A; Faculty of Midwifery and Nursing, University of Medicine and Pharmacy "Carol Davila", 8 Eroilor Sanitari Boulevard, 050474 Bucharest, Romania.
  • Șerban-Sosoi S; Chair of Medical Genetics, University of Medicine and Pharmacy "Carol Davila", 37 Dionisie Lupu Street, 020021 Bucharest, Romania.
  • Pîrvu A; Human Genomics Laboratory, Craiova University of Medicine and Pharmacy, 2-4 Petru Rareș Street, 200349 Craiova, Romania.
  • Streața I; Regional Centre of Medical Genetics Dolj, Clinical Emergency County Hospital, Craiova, 1 Tabaci Street, 200642 Craiova, Romania.
Genes (Basel) ; 13(2)2022 01 24.
Article en En | MEDLINE | ID: mdl-35205257
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Displasia Ectodérmica / Distonía Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Rumanía Pais de publicación: Suiza
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Displasia Ectodérmica / Distonía Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Rumanía Pais de publicación: Suiza