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Small-molecule signal-transduction inhibitors: targeted therapeutic agents for single-gene disorders
_ Small-molecule signal-transduction inhibitors: targeted therapeutic agents for single-gene disorders.
Journal of Medical Genetics:  Mar 19 2010 7:23PM Find similar documents
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Epigenetic signatures of Silver-Russell syndrome
_ Epigenetic signatures of Silver-Russell syndrome.
Journal of Medical Genetics:  Mar 19 2010 7:23PM Find similar documents
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Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable
_ Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable.
Journal of Medical Genetics:  Mar 19 2010 7:23PM Find similar documents
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A cohort study of recurrence patterns among more than 54 000 relatives of oral cleft cases in Denmark: support
_ A cohort study of recurrence patterns among more than 54 000 relatives of oral cleft cases in Denmark: support.
Journal of Medical Genetics:  Mar 19 2010 7:23PM Find similar documents
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Genotype-phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysis
_ Genotype-phenotype correlations in L1 syndrome: a guide for genetic counselling and mutation analysis.
Journal of Medical Genetics:  Mar 19 2010 7:22PM Find similar documents
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A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitivity in a pat
_ A novel splice variant of the DNA-PKcs gene is associated with clinical and cellular radiosensitivity in a pat.
Journal of Medical Genetics:  Mar 19 2010 7:22PM Find similar documents
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Renal tumour suppressor function of the Birt-Hogg-Dube syndrome gene product folliculin
_ Renal tumour suppressor function of the Birt-Hogg-Dube syndrome gene product folliculin.
Journal of Medical Genetics:  Mar 19 2010 7:22PM Find similar documents
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Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
_ Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.
Journal of Medical Genetics:  Mar 19 2010 7:22PM Find similar documents
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Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals
_ Phenotypic spectrum associated with de novo and inherited deletions and duplications at 16p11.2 in individuals.
Journal of Medical Genetics:  Mar 19 2010 7:22PM Find similar documents
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Multiple single nucleotide polymorphisms in the human urate transporter 1 (hURAT1) gene are associated with hy
_ Multiple single nucleotide polymorphisms in the human urate transporter 1 (hURAT1) gene are associated with hy.
Journal of Medical Genetics:  Mar 19 2010 7:22PM Find similar documents

 

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