Your browser doesn't support javascript.
loading
The phenotypic spectrum of proximal 6q deletions based on a large cohort derived from social media and literature reports.
Engwerda, Aafke; Frentz, Barbara; den Ouden, A Lya; Flapper, Boudien C T; Swertz, Morris A; Gerkes, Erica H; Plantinga, Mirjam; Dijkhuizen, Trijnie; van Ravenswaaij-Arts, Conny M A.
Affiliation
  • Engwerda A; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • Frentz B; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • den Ouden AL; Vanboeijen, Assen, The Netherlands.
  • Flapper BCT; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • Swertz MA; Department of Paediatrics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • Gerkes EH; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • Plantinga M; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • Dijkhuizen T; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
  • van Ravenswaaij-Arts CMA; Department of Genetics, University of Groningen, University Medical Centre Groningen, Groningen, The Netherlands.
Eur J Hum Genet ; 26(10): 1478-1489, 2018 10.
Article in En | MEDLINE | ID: mdl-29904178
Subject(s)
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 6 / Developmental Disabilities / Social Media Type of study: Prognostic_studies Limits: Child / Female / Humans / Male Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Países Bajos
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 6 / Developmental Disabilities / Social Media Type of study: Prognostic_studies Limits: Child / Female / Humans / Male Language: En Journal: Eur J Hum Genet Journal subject: GENETICA MEDICA Year: 2018 Document type: Article Affiliation country: Países Bajos