Your browser doesn't support javascript.
loading
Behavioral characteristics associated with 19p13.2 microdeletions.
Welham, Alice; Barth, Bursharan; Moss, Joanna; Penhallow, Jessica; Sheth, Krupa; Wilde, Lucy; Wynn, Sarah; Oliver, Chris.
Affiliation
  • Welham A; University of Birmingham, Birmingham, UK.
  • Barth B; University of Birmingham, Birmingham, UK.
  • Moss J; University of Birmingham, Birmingham, UK.
  • Penhallow J; University of Birmingham, Birmingham, UK.
  • Sheth K; University of Birmingham, Birmingham, UK.
  • Wilde L; University of Birmingham, Birmingham, UK.
  • Wynn S; University of Birmingham, Birmingham, UK.
  • Oliver C; UNIQUE Rare Chromosome Disorder Support Group, London, UK.
Am J Med Genet A ; 167A(10): 2334-43, 2015 Oct.
Article in En | MEDLINE | ID: mdl-26189583
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: Phenotype / Chromosomes, Human, Pair 19 / Chromosome Deletion Type of study: Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: United kingdom Country of publication: United States
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Chromosomes, Human, Pair 19 / Chromosome Deletion Type of study: Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2015 Document type: Article Affiliation country: United kingdom Country of publication: United States