S Goldwurm, A Biondi. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Anemia, Hypochromic/bloodAnemia, Hypochromic/geneticsChildChromosomes, Human, Pair 3Embryonic and Fetal DevelopmentFamily HealthHumansHypospadias/bloodHypospadias/etiologyHypoxia/complicationsHypoxia/congenitalMaleMutationTransferrin/deficiencyTransferrin/genetics
Substances: See more » Transferrin
Year: 2000 PMID: 11102938
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299