Molecular approach to the study of inherited kidney diseases: A way to understand the mechanisms of disease
Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a fam...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
GRÜNFELD, JEAN-PIERRE [verfasserIn] |
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| Format: |
E-Artikel |
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| Erschienen: |
Oxford, UK: Blackwell Publishing Ltd ; 1996 |
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| Schlagwörter: |
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| Umfang: |
Online-Ressource |
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| Reproduktion: |
2007 ; Blackwell Publishing Journal Backfiles 1879-2005 |
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| Übergeordnetes Werk: |
In: Nephrology - Oxford [u.a.] : Wiley-Blackwell, 1995, 2(1996), Seite 0 |
| Übergeordnetes Werk: |
volume:2 ; year:1996 ; pages:0 |
| Links: |
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| DOI / URN: |
10.1111/j.1440-1797.1996.tb00151.x |
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NLEJ241647606 |
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| 520 | |a Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. | ||
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10.1111/j.1440-1797.1996.tb00151.x doi (DE-627)NLEJ241647606 DE-627 ger DE-627 rakwb GRÜNFELD, JEAN-PIERRE verfasserin aut Molecular approach to the study of inherited kidney diseases: A way to understand the mechanisms of disease Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Alport's syndrome In Nephrology Oxford [u.a.] : Wiley-Blackwell, 1995 2(1996), Seite 0 Online-Ressource (DE-627)NLEJ243925859 (DE-600)2008235-6 1440-1797 nnns volume:2 year:1996 pages:0 http://dx.doi.org/10.1111/j.1440-1797.1996.tb00151.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1996 0 |
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10.1111/j.1440-1797.1996.tb00151.x doi (DE-627)NLEJ241647606 DE-627 ger DE-627 rakwb GRÜNFELD, JEAN-PIERRE verfasserin aut Molecular approach to the study of inherited kidney diseases: A way to understand the mechanisms of disease Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Alport's syndrome In Nephrology Oxford [u.a.] : Wiley-Blackwell, 1995 2(1996), Seite 0 Online-Ressource (DE-627)NLEJ243925859 (DE-600)2008235-6 1440-1797 nnns volume:2 year:1996 pages:0 http://dx.doi.org/10.1111/j.1440-1797.1996.tb00151.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1996 0 |
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10.1111/j.1440-1797.1996.tb00151.x doi (DE-627)NLEJ241647606 DE-627 ger DE-627 rakwb GRÜNFELD, JEAN-PIERRE verfasserin aut Molecular approach to the study of inherited kidney diseases: A way to understand the mechanisms of disease Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Alport's syndrome In Nephrology Oxford [u.a.] : Wiley-Blackwell, 1995 2(1996), Seite 0 Online-Ressource (DE-627)NLEJ243925859 (DE-600)2008235-6 1440-1797 nnns volume:2 year:1996 pages:0 http://dx.doi.org/10.1111/j.1440-1797.1996.tb00151.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1996 0 |
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10.1111/j.1440-1797.1996.tb00151.x doi (DE-627)NLEJ241647606 DE-627 ger DE-627 rakwb GRÜNFELD, JEAN-PIERRE verfasserin aut Molecular approach to the study of inherited kidney diseases: A way to understand the mechanisms of disease Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Alport's syndrome In Nephrology Oxford [u.a.] : Wiley-Blackwell, 1995 2(1996), Seite 0 Online-Ressource (DE-627)NLEJ243925859 (DE-600)2008235-6 1440-1797 nnns volume:2 year:1996 pages:0 http://dx.doi.org/10.1111/j.1440-1797.1996.tb00151.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1996 0 |
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10.1111/j.1440-1797.1996.tb00151.x doi (DE-627)NLEJ241647606 DE-627 ger DE-627 rakwb GRÜNFELD, JEAN-PIERRE verfasserin aut Molecular approach to the study of inherited kidney diseases: A way to understand the mechanisms of disease Oxford, UK Blackwell Publishing Ltd 1996 Online-Ressource nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. 2007 Blackwell Publishing Journal Backfiles 1879-2005 |2007|||||||||| Alport's syndrome In Nephrology Oxford [u.a.] : Wiley-Blackwell, 1995 2(1996), Seite 0 Online-Ressource (DE-627)NLEJ243925859 (DE-600)2008235-6 1440-1797 nnns volume:2 year:1996 pages:0 http://dx.doi.org/10.1111/j.1440-1797.1996.tb00151.x text/html Verlag Deutschlandweit zugänglich Volltext GBV_USEFLAG_U ZDB-1-DJB GBV_NL_ARTICLE AR 2 1996 0 |
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Molecular approach to the study of inherited kidney diseases: A way to understand the mechanisms of disease |
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Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. |
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Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. |
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Summary: Recent progress in molecular genetics has provided understanding of the molecular mechanisms of inherited disorders (and also of more general mechanisms). This progress is first based on good clinical observations, as was recently demonstrated in the identification of the PKD1 gene in a family with a chromosomal translocation. These advances are also of value for better classification of hereditary diseases and for better genetic counselling of the affected families, as shown in Alport's syndrome. |
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