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- W1504041709 endingPage "457" @default.
- W1504041709 startingPage "441" @default.
- W1504041709 abstract "It is increasingly recognized that mutations in genes and pathways critical for left‐right (L‐R) patterning are involved in common isolated congenital malformations such as congenital heart disease, biliary tract anomalies, renal polycystic disease, and malrotation of the intestine, indicating that disorders of L‐R development are far more common than a 1 in 10,000 incidence of heterotaxia might suggest. Understanding L‐R patterning disorders requires knowledge of molecular biology, embryology, pediatrics, and internal medicine and is relevant to day‐to‐day clinical genetics practice. We have reviewed data from mammalian (human and mouse) L‐R patterning disorders to provide a clinically oriented perspective that might afford the clinician or researcher additional insights into this diagnostically challenging area." @default.
- W1504041709 created "2016-06-24" @default.
- W1504041709 creator A5024781173 @default.
- W1504041709 creator A5072159584 @default.
- W1504041709 date "2004-05-18" @default.
- W1504041709 modified "2023-10-14" @default.
- W1504041709 title "Breaking symmetry: a clinical overview of left-right patterning" @default.
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