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Clinical Genetics
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April 19, 2003
Detection of five new mutations in the APC gene using denaturing high-performance liquid chromatography
W Heinritz, A Kujat, U G Froster
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
November 25, 2003
[Molecular genetic mutation analysis of the PTPN11 gene in the multiple lentigines (LEOPARD) syndrome]
U G Froster, H-J Glander, W Heinritz
Der Orthopade
|
March 2, 2005
[Hereditary multiple exostoses. Molecular genetic analysis of the EXT1 gene in an unusual family]
W Heinritz, M Pretzsch, S Koall, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 17, 2008
A new mutation in the GJB3 gene in a patient with erythrokeratodermia variabilis
R Renner, U Paasch, J C Simon, et al.
Prenatal Diagnosis
|
May 28, 2004
Another case of autosomal dominant exstrophy of the bladder
U G Froster, W Heinritz, J Bennek, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 26, 2009
Multiple trichoepitheliomas--a novel mutation in the CYLD gene
C Amaro, I Freitas, P Lamarão, et al.
Annals of Human Genetics
|
October 3, 2007
Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC)
W Heinritz, U Paasch, M Sticherling, et al.
European Journal of Pain (London, England)
|
June 24, 2018
Mutation in Na<sub>v</sub> 1.7 causes high olfactory sensitivity
A Haehner, T Hummel, W Heinritz, et al.
Placenta
|
June 12, 2004
Pre-eclampsia as a 'three stage problem'--a workshop report
H Stepan, R Faber, U G Froster, et al.
The British Journal of Dermatology
|
April 26, 2006
A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene
W Heinritz, S Grunewald, S Strenge, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 15) with videos related to
Sort By:
Page
of 2
Clinical Genetics
|
April 19, 2003
Detection of five new mutations in the APC gene using denaturing high-performance liquid chromatography
W Heinritz, A Kujat, U G Froster
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
November 25, 2003
[Molecular genetic mutation analysis of the PTPN11 gene in the multiple lentigines (LEOPARD) syndrome]
U G Froster, H-J Glander, W Heinritz
Der Orthopade
|
March 2, 2005
[Hereditary multiple exostoses. Molecular genetic analysis of the EXT1 gene in an unusual family]
W Heinritz, M Pretzsch, S Koall, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 17, 2008
A new mutation in the GJB3 gene in a patient with erythrokeratodermia variabilis
R Renner, U Paasch, J C Simon, et al.
Prenatal Diagnosis
|
May 28, 2004
Another case of autosomal dominant exstrophy of the bladder
U G Froster, W Heinritz, J Bennek, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 26, 2009
Multiple trichoepitheliomas--a novel mutation in the CYLD gene
C Amaro, I Freitas, P Lamarão, et al.
Annals of Human Genetics
|
October 3, 2007
Evidence for a founder effect of the germline fumarate hydratase gene mutation R58P causing hereditary leiomyomatosis and renal cell cancer (HLRCC)
W Heinritz, U Paasch, M Sticherling, et al.
European Journal of Pain (London, England)
|
June 24, 2018
Mutation in Na<sub>v</sub> 1.7 causes high olfactory sensitivity
A Haehner, T Hummel, W Heinritz, et al.
Placenta
|
June 12, 2004
Pre-eclampsia as a 'three stage problem'--a workshop report
H Stepan, R Faber, U G Froster, et al.
The British Journal of Dermatology
|
April 26, 2006
A case of Brooke-Spiegler syndrome with a new mutation in the CYLD gene
W Heinritz, S Grunewald, S Strenge, et al.
Page
of 2