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F H Herrmann

Showing results (31-40 of 66) with videos related to

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Journal of Neurology|April 1, 1987
Atypical form of X-linked proximal pseudohypertrophic muscular dystrophyA W Spiegler, I Hausmanowa-Petrusewicz, J Borkowska, et al.
Clinical Genetics|September 1, 1988
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicF H Herrmann, K Wulff, M Wehnert, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1988
First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDRF H Herrmann, T Kruse, M Wehnert, et al.
Thrombosis Research|December 15, 1983
Glycoprotein IIb-IIIa complex in platelets of patients and heterozygotes of Glanzmann's thrombastheniaF H Herrmann, M Meyer, G O Gogstad, et al.
Virchows Archiv : an International Journal of Pathology|December 22, 1999
Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma: FISH deletion screening with YAC DNA probesM Poetsch, C Woenckhaus, T Dittberner, et al.
Cancer Genetics and Cytogenetics|July 17, 1998
An increased frequency of numerical chromosomal abnormalities and 1p36 deletions in isolated cells from paraffin sections of malignant melanomas by means of interphase cytogeneticsM Poetsch, C Woenckhaus, T Dittberner, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|October 4, 2000
First hints for a correlation between amplification of the Int-2 gene and infection with human papillomavirus in head and neck squamous cell carcinomasB Kleist, M Poetsch, A Bankau, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 5, 1998
Differences in chromosomal aberrations between nodular and superficial spreading malignant melanoma detected by interphase cytogeneticsM Poetsch, C Woenckhaus, T Dittberner, et al.
Pediatric Hematology and Oncology|May 3, 2006
Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->AU Hennewig, S Eisert, K Wulff, et al.
Journal of Dental Research|February 25, 2003
The interleukin-1 polymorphism, smoking, and the risk of periodontal disease in the population-based SHIP studyP Meisel, A Siegemund, R Grimm, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
Journal of Neurology|April 1, 1987
Atypical form of X-linked proximal pseudohypertrophic muscular dystrophyA W Spiegler, I Hausmanowa-Petrusewicz, J Borkowska, et al.
Clinical Genetics|September 1, 1988
Haplotype analysis of classical and mild phenotype of phenylketonuria in the German Democratic RepublicF H Herrmann, K Wulff, M Wehnert, et al.
Folia Haematologica (Leipzig, Germany : 1928)|January 1, 1988
First experiences in application of RFLP analysis for carrier detection in preparation of prenatal diagnosis of hemophilia A in the GDRF H Herrmann, T Kruse, M Wehnert, et al.
Thrombosis Research|December 15, 1983
Glycoprotein IIb-IIIa complex in platelets of patients and heterozygotes of Glanzmann's thrombastheniaF H Herrmann, M Meyer, G O Gogstad, et al.
Virchows Archiv : an International Journal of Pathology|December 22, 1999
Significance of the small subtelomeric area of chromosome 1 (1p36.3) in the progression of malignant melanoma: FISH deletion screening with YAC DNA probesM Poetsch, C Woenckhaus, T Dittberner, et al.
Cancer Genetics and Cytogenetics|July 17, 1998
An increased frequency of numerical chromosomal abnormalities and 1p36 deletions in isolated cells from paraffin sections of malignant melanomas by means of interphase cytogeneticsM Poetsch, C Woenckhaus, T Dittberner, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|October 4, 2000
First hints for a correlation between amplification of the Int-2 gene and infection with human papillomavirus in head and neck squamous cell carcinomasB Kleist, M Poetsch, A Bankau, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|August 5, 1998
Differences in chromosomal aberrations between nodular and superficial spreading malignant melanoma detected by interphase cytogeneticsM Poetsch, C Woenckhaus, T Dittberner, et al.
Pediatric Hematology and Oncology|May 3, 2006
Long-term FVII substitution in a preterm infant with severe gastrointestinal bleeding and FVII deficiency due to a homozygous donor splice mutation IVS4+1G-->AU Hennewig, S Eisert, K Wulff, et al.
Journal of Dental Research|February 25, 2003
The interleukin-1 polymorphism, smoking, and the risk of periodontal disease in the population-based SHIP studyP Meisel, A Siegemund, R Grimm, et al.
Pageof 7