Your browser doesn't support javascript.
loading
Club foot in association with the 22q11.2 deletion syndrome: An observational study.
Homans, Jelle F; Crowley, Terrence B; Chen, Erin; McGinn, Daniel E; Deeney, Vincent F X; Sakkers, Ralph J B; Davidson, Richard S; Castelein, René M; McDonald-McGinn, Donna M.
Affiliation
  • Homans JF; Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Crowley TB; Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.
  • Chen E; Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.
  • McGinn DE; Division of Human Genetics and 22q and You Center, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.
  • Deeney VFX; Department of Orthopaedic Surgery, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.
  • Sakkers RJB; The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Davidson RS; Department of Orthopaedic Surgery, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Castelein RM; Department of Orthopaedic Surgery, The Children's Hospital of Philadelphia (CHOP), Philadelphia, Pennsylvania.
  • McDonald-McGinn DM; The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, Pennsylvania.
Am J Med Genet A ; 176(10): 2135-2139, 2018 10.
Article in En | MEDLINE | ID: mdl-30380189
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Clubfoot / DiGeorge Syndrome Type of study: Observational_studies / Risk_factors_studies Limits: Humans / Male / Newborn Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2018 Type: Article Affiliation country: Netherlands
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Clubfoot / DiGeorge Syndrome Type of study: Observational_studies / Risk_factors_studies Limits: Humans / Male / Newborn Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2018 Type: Article Affiliation country: Netherlands