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M Stumm

Showing results (31-40 of 57) with videos related to

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Anticancer Research|June 12, 1999
The differential expression of proinflammatory cytokines IL-6, IL-8 and TNF-alpha in renal cell carcinomaB König, F Steinbach, B Janocha, et al.
Osteoarthritis and Cartilage|June 16, 2012
Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCRM Stumm, E Boger, C G Gaissmaier, et al.
Human Genetics|August 14, 2001
Improved definition of chromosomal breakpoints using high-resolution multicolour bandingJ Lemke, I Chudoba, G Senger, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 26, 2010
The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal ageA Hagen, M Entezami, A Gasiorek-Wiens, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Frequency of CFTR gene mutations in males participating in an ICSI programmeS Jakubiczka, T Bettecken, M Stumm, et al.
American Journal of Human Genetics|October 1, 1995
The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1M Stumm, R A Gatti, A Reis, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancyO Bartsch, A Wagner, G K Hinkel, et al.
European Journal of Pediatrics|October 5, 2001
Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short statureJ Musebeck, K Mohnike, P Beye, et al.
Prenatal Diagnosis|October 20, 2000
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.
Journal of Medical Genetics|June 19, 2002
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probesA Weise, H Starke, A Heller, et al.
Pageof 6

Showing results (31-40 of 57) with videos related to

Sort By:
Pageof 6
Anticancer Research|June 12, 1999
The differential expression of proinflammatory cytokines IL-6, IL-8 and TNF-alpha in renal cell carcinomaB König, F Steinbach, B Janocha, et al.
Osteoarthritis and Cartilage|June 16, 2012
Genomic chondrocyte culture profiling by array-CGH, interphase-FISH and RT-PCRM Stumm, E Boger, C G Gaissmaier, et al.
Human Genetics|August 14, 2001
Improved definition of chromosomal breakpoints using high-resolution multicolour bandingJ Lemke, I Chudoba, G Senger, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|October 26, 2010
The impact of first trimester screening and early fetal anomaly scan on invasive testing rates in women with advanced maternal ageA Hagen, M Entezami, A Gasiorek-Wiens, et al.
Human Reproduction (Oxford, England)|July 13, 1999
Frequency of CFTR gene mutations in males participating in an ICSI programmeS Jakubiczka, T Bettecken, M Stumm, et al.
American Journal of Human Genetics|October 1, 1995
The ataxia-telangiectasia-variant genes 1 and 2 are distinct from the ataxia-telangiectasia gene on chromosome 11q23.1M Stumm, R A Gatti, A Reis, et al.
European Journal of Human Genetics : EJHG|November 26, 1999
FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancyO Bartsch, A Wagner, G K Hinkel, et al.
European Journal of Pediatrics|October 5, 2001
Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short statureJ Musebeck, K Mohnike, P Beye, et al.
Prenatal Diagnosis|October 20, 2000
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.
Journal of Medical Genetics|June 19, 2002
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probesA Weise, H Starke, A Heller, et al.
Pageof 6