O W Quarrell, E L Maltby, C J Harrison. Show Affiliations »
Abstract
Entities: Disease
Mesh： See more » Abnormalities, Multiple/geneticsChromosome BreakageConsanguinityCraniosynostoses/geneticsFanconi Anemia/diagnosisFanconi Anemia/geneticsFollow-Up StudiesHumansInfantKaryotypingMaleSyndrome
Year: 1998 PMID： 9450894 DOI： 10.1002/(sici)1096-8628(19980113)75:2<228::aid-ajmg25>3.0.co;2-q
Source DB: PubMed Journal: Am J Med Genet ISSN： 0148-7299