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Original research
Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndrome

Authors

  • Joan Sabria-Back BCNatal, Barcelona Center for Maternal-Fetal and Neonatal Medicine, Hospital Sant Joan de Déu and Hospital Clinic, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Ana Monteagudo-Sánchez Cancer Epigenetics and Biology Program, Bellvitge Institute for Biomedical Research, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Marta Sánchez-Delgado Cancer Epigenetics and Biology Program, Bellvitge Institute for Biomedical Research, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Anne C Ferguson-Smith Department of Genetics, University of Cambridge, Cambridge, Cambridgeshire, UK PubMed articlesGoogle scholar articles
  • Olga Gómez BCNatal, Barcelona Center for Maternal-Fetal and Neonatal Medicine, Hospital Sant Joan de Déu and Hospital Clinic, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Africa Pertierra Cartada BCNatal, Barcelona Center for Maternal-Fetal and Neonatal Medicine, Hospital Sant Joan de Déu and Hospital Clinic, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Jair Tenorio INGEMM (Instituto de Genética Médica y Molecular), Hospital Universitario La Paz-IdiPaz, Hospital universitario la Paz, Madrid, SpainCIBERER (Centro de Investigación Biomédica en Red de Enfermedades Raras), Madrid, SpainITHACA, European Reference Network on Rare Congenital Malformations and Rare Intellectual Disabilities, Madrid, Spain PubMed articlesGoogle scholar articles
  • Julián Nevado INGEMM (Instituto de Genética Médica y Molecular), Hospital Universitario La Paz-IdiPaz, Hospital universitario la Paz, Madrid, SpainCIBERER (Centro de Investigación Biomédica en Red de Enfermedades Raras), Madrid, SpainITHACA, European Reference Network on Rare Congenital Malformations and Rare Intellectual Disabilities, Madrid, Spain PubMed articlesGoogle scholar articles
  • Pablo Lapunzina INGEMM (Instituto de Genética Médica y Molecular), Hospital Universitario La Paz-IdiPaz, Hospital universitario la Paz, Madrid, SpainCIBERER (Centro de Investigación Biomédica en Red de Enfermedades Raras), Madrid, SpainITHACA, European Reference Network on Rare Congenital Malformations and Rare Intellectual Disabilities, Madrid, Spain PubMed articlesGoogle scholar articles
  • Arrate Pereda Aguirre Molecular (Epi)Genetics Laboratory, Bioaraba Health Research Institute, Vitoria-Gasteiz, Spain PubMed articlesGoogle scholar articles
  • Carles Giménez Sevilla Reprogenetics, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Estefanía Toro Toro Reprogenetics, Barcelona, Spain PubMed articlesGoogle scholar articles
  • Guiomar Perez de Nanclares Molecular (Epi)Genetics Laboratory, Bioaraba Health Research Institute, Vitoria-Gasteiz, Spain PubMed articlesGoogle scholar articles
  • David Monk Cancer Epigenetics and Biology Program, Bellvitge Institute for Biomedical Research, Barcelona, SpainBiomedical Research Center, School of Biological Sciences, University of East Anglia, Norwich, UK PubMed articlesGoogle scholar articles
  1. Correspondence to Dr David Monk, University of East Anglia, Norwich NR4 7TJ, UK; d.monk{at}uea.ac.uk
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Citation

Sabria-Back J, Monteagudo-Sánchez A, Sánchez-Delgado M, et al
Preimplantation genetic testing for a chr14q32 microdeletion in a family with Kagami-Ogata syndrome and Temple syndrome

Publication history

  • Received August 27, 2020
  • Revised December 8, 2020
  • Accepted December 13, 2020
  • First published February 12, 2021.

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