Pages that link to "Q42553858"
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The following pages link to Prenatal diagnosis in congenital erythropoietic porphyria by metabolic measurement and DNA mutation analysis (Q42553858):
Displaying 11 items.
- Genetic defects in the porphyrias: types and significance (Q28268491) (← links)
- The cutaneous porphyrias: a review. The British Photodermatology Group (Q33610809) (← links)
- Congenital erythropoietic porphyria: advances in pathogenesis and treatment (Q34680808) (← links)
- Congenital Erythropoietic Porphyria: Characterization of Murine Models of the Severe Common (C73R/C73R) and Later-Onset Genotypes (Q35136687) (← links)
- Diagnosis and management of the erythropoietic porphyrias (Q35200021) (← links)
- Porphyria Diagnostics-Part 1: A Brief Overview of the Porphyrias (Q36267789) (← links)
- Role of genetic testing in the management of patients with inherited porphyria and their families (Q38100668) (← links)
- How genetic defects are identified (Q41745493) (← links)
- Mutational analysis of uroporphyrinogen III cosynthase gene in Iranian families with congenital erythropoietic porphyria (Q44005499) (← links)
- Congenital erythropoietic porphyria (Günther's disease): two cases with very early prenatal manifestation and cystic hygroma (Q44282035) (← links)
- Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese family. (Q54564092) (← links)