O Mutchinick. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChildChild, PreschoolChromosomes, Human, 21-22 and YConsanguinityDermatoglyphicsFacial ExpressionFemaleGenes, RecessiveHumansIntellectual Disability/geneticsLymphocytes/cytologyMotor ActivityMouth Mucosa/cytologyPedigreeSex ChromatinSpeech Disorders/geneticsSyndrome
Year: 1972 PMID: 5025484 PMCID: PMC1469223 DOI: 10.1136/jmg.9.1.60
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318