E M Thompson, B N Harding, B D Lake, S C Smith. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Abnormalities, Multiple/pathologyBrain/pathologyDigestive System/pathologyGenetic LinkageIntellectual Disability/pathologyMaleMuscles/pathologySyndromeX Chromosome
Year: 1986 PMID: 3746847 PMCID: PMC1049715 DOI: 10.1136/jmg.23.4.372
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318