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1. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.

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2. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.


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3. Genetische Aspekte des familiären Morbus Menière


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4. RB1 gene mutations in peripheral blood DNA of patients with isolated unilateral retinoblastoma.

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5. A PCR test for the detection of hypermethylated alleles at the retinoblastoma locus

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6. Detection of homozygous deletions in tumors by hybridization of representational difference analysis (RDA) products to chromosome-specific YAC clone arrays.

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7. Somatic mosaicism in a patient with bilateral retinoblastoma.

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8. Identification of deletions in the human low density lipoprotein receptor gene.

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9. Identification of deletions in the human low density lipoprotein receptor gene.


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10. Detection of homozygous deletions in tumors by hybridization of representational difference analysis (RDA) products to chromosome- specific YAC clone arrays


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