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A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X
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Zeitschriftentitel: | Human Mutation |
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Personen und Körperschaften: | , , , , |
In: | Human Mutation, 19, 2002, 4, S. 462-462 |
Format: | E-Article |
Sprache: | Englisch |
veröffentlicht: |
Hindawi Limited
|
Schlagwörter: |
author_facet |
Heathcott, Rosemary W. Morison, Ian M. Gubler, Marie Claire Corbett, Robin Reeve, Anthony E. Heathcott, Rosemary W. Morison, Ian M. Gubler, Marie Claire Corbett, Robin Reeve, Anthony E. |
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author |
Heathcott, Rosemary W. Morison, Ian M. Gubler, Marie Claire Corbett, Robin Reeve, Anthony E. |
spellingShingle |
Heathcott, Rosemary W. Morison, Ian M. Gubler, Marie Claire Corbett, Robin Reeve, Anthony E. Human Mutation A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X Genetics (clinical) Genetics |
author_sort |
heathcott, rosemary w. |
spelling |
Heathcott, Rosemary W. Morison, Ian M. Gubler, Marie Claire Corbett, Robin Reeve, Anthony E. 1059-7794 1098-1004 Hindawi Limited Genetics (clinical) Genetics http://dx.doi.org/10.1002/humu.9031 A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X Human Mutation |
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10.1002/humu.9031 |
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Hindawi Limited, 2002 |
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Human Mutation |
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title |
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_unstemmed |
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_full |
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_fullStr |
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_full_unstemmed |
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_short |
A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_sort |
a review of the phenotypic variation due to the denys-drash syndrome-associated germlinewt1 mutation r362x |
topic |
Genetics (clinical) Genetics |
url |
http://dx.doi.org/10.1002/humu.9031 |
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2002 |
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462-462 |
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author | Heathcott, Rosemary W., Morison, Ian M., Gubler, Marie Claire, Corbett, Robin, Reeve, Anthony E. |
author_facet | Heathcott, Rosemary W., Morison, Ian M., Gubler, Marie Claire, Corbett, Robin, Reeve, Anthony E., Heathcott, Rosemary W., Morison, Ian M., Gubler, Marie Claire, Corbett, Robin, Reeve, Anthony E. |
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spelling | Heathcott, Rosemary W. Morison, Ian M. Gubler, Marie Claire Corbett, Robin Reeve, Anthony E. 1059-7794 1098-1004 Hindawi Limited Genetics (clinical) Genetics http://dx.doi.org/10.1002/humu.9031 A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X Human Mutation |
spellingShingle | Heathcott, Rosemary W., Morison, Ian M., Gubler, Marie Claire, Corbett, Robin, Reeve, Anthony E., Human Mutation, A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X, Genetics (clinical), Genetics |
title | A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_full | A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_fullStr | A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_full_unstemmed | A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_short | A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
title_sort | a review of the phenotypic variation due to the denys-drash syndrome-associated germlinewt1 mutation r362x |
title_unstemmed | A review of the phenotypic variation due to the Denys-Drash syndrome-associated germlineWT1 mutation R362X |
topic | Genetics (clinical), Genetics |
url | http://dx.doi.org/10.1002/humu.9031 |