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Three new families with arterial tortuosity syndrome
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FAME: Flood risk and damage assessment using modelling and earth observation techniques
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Homozygosity mapping of a gene for arterial tortuosity syndrome to chromosome 20q13
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Homozygosity mapping of a gene for arterial tortuosity snydrome
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Identification of a new connexin gene GJA11 (Cx59) using degenerate PCR primers
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Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNA(Ser(UCN)) gene
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Refined physical mapping and genomic structure of the EXTL1 gene.
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Complete genomic structure and mutational spectrum of PHKA2 in patients with X-linked liver glycogenosis type I and II.
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CAG repeat contraction in the androgen receptor gene in three brothers with mental retardation.
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On-line data acquisition