Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration

By Grech V.  

Human Molecular Genetics, Vol. 11, Iss. 4, 2002-02 ,pp. : 379-388

Oxford University Press

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Genotype–phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype

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Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1263-1271

Oxford University Press

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Of mice and (wo)men: genotype–phenotype correlations in BRCA1

By Hohenstein Peter  

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-10 ,pp. : 271-277

Oxford University Press

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Of mice and (wo)men: genotype–phenotype correlations in BRCA1

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Human Molecular Genetics, Vol. 13, Iss. 4, 2004-02 ,pp. : 473-473

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PTEN mutation spectrum and genotype–phenotype correlations in Bannayan–Riley–Ruvalcaba syndrome suggest a single entity with Cowden syndrome

By Marsh Debbie J.   Kum Jennifer B.   Lunetta Kathryn L.  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1461-1472

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