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Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype-Phenotype Correlation.
Gavril, Eva-Cristiana; Popescu, Roxana; Nuca, Irina; Ciobanu, Cristian-Gabriel; Butnariu, Lacramioara Ionela; Rusu, Cristina; Pânzaru, Monica-Cristina.
Afiliación
  • Gavril EC; Department of Medical Genetics, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, University Street, No 16, 700115 Iasi, Romania.
  • Popescu R; Investigații Medicale Praxis, St. Moara de Vant No 35, 700376 Iasi, Romania.
  • Nuca I; Department of Medical Genetics, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, University Street, No 16, 700115 Iasi, Romania.
  • Ciobanu CG; Department of Medical Genetics "Saint Mary" Emergency Children's Hospital, St. Vasile Lupu No 62, 700309 Iasi, Romania.
  • Butnariu LI; Department of Medical Genetics, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, University Street, No 16, 700115 Iasi, Romania.
  • Rusu C; Investigații Medicale Praxis, St. Moara de Vant No 35, 700376 Iasi, Romania.
  • Pânzaru MC; Department of Medical Genetics, Faculty of Medicine, "Grigore T. Popa" University of Medicine and Pharmacy, University Street, No 16, 700115 Iasi, Romania.
Genes (Basel) ; 13(11)2022 11 10.
Article en En | MEDLINE | ID: mdl-36360320
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Rumanía
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Síndrome de DiGeorge Tipo de estudio: Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Genes (Basel) Año: 2022 Tipo del documento: Article País de afiliación: Rumanía