Your browser doesn't support javascript.
loading
A newly recognized syndrome of severe growth deficiency, microcephaly, intellectual disability, and characteristic facial features.
Vinkler, Chana; Leshinsky-Silver, Esther; Michelson, Marina; Haas, Dorothea; Lerman-Sagie, Tally; Lev, Dorit.
Affiliation
  • Vinkler C; Institute of Medical Genetics, Wolfson Medical Center, Holon, Israel; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel. Electronic address: vinkler2@gmail.com.
  • Leshinsky-Silver E; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Molecular Genetics Laboratory, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Michelson M; Institute of Medical Genetics, Wolfson Medical Center, Holon, Israel; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel.
  • Haas D; Division of Inborn Metabolic Diseases, University Children's Hospital, Im Neuenheimer Feld, Heidelberg, Germany.
  • Lerman-Sagie T; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Pediatric Neurology Unit, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Lev D; Institute of Medical Genetics, Wolfson Medical Center, Holon, Israel; Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel; Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel. Electronic address: dorlev@post.tau.ac.il.
Eur J Med Genet ; 57(6): 288-92, 2014.
Article in En | MEDLINE | ID: mdl-24709618
Subject(s)
Key words
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Abnormalities, Multiple / Face / Growth Disorders / Intellectual Disability / Microcephaly Limits: Child / Female / Humans Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2014 Type: Article
Fulltext
Add to My VHL
Print
XML
PubMed Links
Search on Google

Full text: 1 Database: MEDLINE Main subject: Abnormalities, Multiple / Face / Growth Disorders / Intellectual Disability / Microcephaly Limits: Child / Female / Humans Language: En Journal: Eur J Med Genet Journal subject: GENETICA MEDICA Year: 2014 Type: Article