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Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA)
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1992
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GeneticsImmunodeficienciesGenetic EpidemiologyHuman PolymorphismMolecular BiologyPathologyMills DivisionMolecular GeneticsDisease Gene IdentificationGenomicsGenetic MedicineClinical GeneticsGenetic AnalysisPublic HealthChromosome 9Tetranucleotide Repeat PolymorphismMonogenic DisordersInherited Metabolic DiseaseDeeann Even DivisionAllelic VariantGenetic DisorderMedical GeneticsMedicineUsa Search
Journal Article Tetranucleotide repeat polymorphism at the human alpha fibrinogen locus (FGA) Get access Kathleen A. Mills, Kathleen A. Mills Division of Medicai Genetics, Department of Pediatrics, University of Iowa Hospitals and ClinicsIowa City, IA 52242, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar DeeAnn Even, DeeAnn Even Division of Medicai Genetics, Department of Pediatrics, University of Iowa Hospitals and ClinicsIowa City, IA 52242, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Jeffray C. Murray Jeffray C. Murray * Division of Medicai Genetics, Department of Pediatrics, University of Iowa Hospitals and ClinicsIowa City, IA 52242, USA * To whom correspondence should be addressed Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 1, Issue 9, December 1992, Page 779, https://doi.org/10.1093/hmg/1.9.779 Published: 01 December 1992