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Familial renal cell carcinoma: clinical and molecular genetic aspects.
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Hereditary spastic paraplegia: clinical-genetic characteristics and evolving molecular mechanisms.
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Impact of MS genetic loci on familial aggregation, clinical phenotype, and disease prediction.
Primary familial brain calcification: Genetic analysis and clinical spectrum.
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Benign familial neonatal convulsions: evidence for clinical and genetic heterogeneity.
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Hereditary (familial) renal disease: clinical and genetic studies.
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Recommend Documents
Familial renal cell carcinoma: clinical and molecular genetic aspects.
Clinical and genetic correlations of familial Hirschsprung's disease.
A clinical and genetic study of familial Parkinson's disease.
Hereditary hemolytic anemia with erythrocyte pyrimidine 5'-nucleotidase deficiency in Spain. Clinical, biological and familial studies.
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Cytogenetic and molecular studies of a familial renal cell carcinoma.
Potential genetic anticipation in hereditary leiomyomatosis-renal cell cancer (HLRCC).
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