A splice site mutation in HERC1 leads to syndromic intellectual disability with macrocephaly and facial dysmorphism: Further delineation of the phenotypic spectrum

No abstract is available for this paper.

• Publication year

  2016

• Venue

  American Journal of Medical Genetics. Part A

• Publication date

  2016-04-25

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/ajmg.a.37654PMID 27108999
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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