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H.H. Ropers

Radboud University Nijmegen

47

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horm one receptor gene

1995
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Mapping of the choroideremia-like (CHML) gene at 1q42-qter and mutation analysis in patients with Usher syndrome type II

1994 Genomics
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Genomic Organization and Chromosomal Assignment of the Human Voltage-Gated Na+ Channel β1 Subunit Gene (SCN1B)

1994 Genomics
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X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism

1993 American Journal of Human Genetics
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Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A

1993 Science
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Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints

1993 Human Genetics
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Isolation of a candidate gene for Norrie disease by positional cloning.

1992 Nature Genetics
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Generation and characterization of radiation reduced cell hybrids and isolation of probes from the proximal short arm of the human X chromosome.

1992 Human Genetics
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Report of the Second International Workshop on Human Chromosome 19 Mapping 1992

1992 Cytogenetic and Genome Research
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Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)

1992 American Journal of Human Genetics
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Citations (31)