Your browser doesn't support javascript.
loading
Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder.
Bhat, Gifty; LaGrave, Danielle; Millson, Alison; Herriges, John; Lamb, Allen N; Matalon, Reuben.
Affiliation
  • Bhat G; Division of Genetic Medicine, The Children's Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY, USA. Electronic address: drgiftybhat@gmail.com.
  • LaGrave D; ARUP Laboratories, Salt Lake City, UT, USA.
  • Millson A; ARUP Laboratories, Salt Lake City, UT, USA.
  • Herriges J; ARUP Laboratories, Salt Lake City, UT, USA; Department of Pathology, University of Utah, Salt Lake City, UT, USA.
  • Lamb AN; ARUP Laboratories, Salt Lake City, UT, USA; Department of Pathology, University of Utah, Salt Lake City, UT, USA.
  • Matalon R; Pediatric Genetics, University of Texas Medical Branch, Galveston, TX, USA.
Eur J Med Genet ; 59(9): 470-3, 2016 Sep.
Article in En | MEDLINE | ID: mdl-27238888
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, X / Rho Guanine Nucleotide Exchange Factors / Autism Spectrum Disorder Limits: Child / Female / Humans / Newborn / Pregnancy Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2016 Document type: Article Country of publication: Netherlands
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Chromosomes, Human, X / Rho Guanine Nucleotide Exchange Factors / Autism Spectrum Disorder Limits: Child / Female / Humans / Newborn / Pregnancy Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2016 Document type: Article Country of publication: Netherlands