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M Zenker

Showing results (41-50 of 57) with videos related to

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Clinical Genetics|July 30, 2011
Two novel germline KRAS mutations: expanding the molecular and clinical phenotypeZ Stark, G Gillessen-Kaesbach, M M Ryan, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A novel mutation in the FRAS1 gene in a patient with Fraser syndromeS Ozemri Sag, O Gorukmez, O Gorukmez, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|August 10, 2012
Cellular and molecular properties of (90)Y-labeled cetuximab in combination with radiotherapy on human tumor cells in vitroM Saki, M Toulany, W Sihver, et al.
Clinical Genetics|March 17, 2012
Clinical and molecular analysis of RASopathies in a group of Turkish patientsP Ö Şimşek-Kiper, Y Alanay, B Gülhan, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|August 30, 2012
Flow cytometric cell-based assay to preselect antibody constructs for radionuclide conjugationM Ingargiola, C Dittfeld, R Runge, et al.
Leukemia|March 16, 2007
Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndromeA Karow, D Steinemann, G Göhring, et al.
Clinical Genetics|January 31, 2012
A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same familyW Y Ng, F Pasutto, T M Bardakjian, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 5, 2008
Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation - functional evidence for a hydrophobic side-chain?B Utsch, I Brun-Heath, G Staatz, et al.
American Journal of Human Genetics|October 16, 1999
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasiaI Quack, B Vonderstrass, M Stock, et al.
Kidney International|August 17, 2006
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disordersK Hasselbacher, R C Wiggins, V Matejas, et al.
Pageof 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
Clinical Genetics|July 30, 2011
Two novel germline KRAS mutations: expanding the molecular and clinical phenotypeZ Stark, G Gillessen-Kaesbach, M M Ryan, et al.
Genetic Counseling (Geneva, Switzerland)|June 6, 2015
A novel mutation in the FRAS1 gene in a patient with Fraser syndromeS Ozemri Sag, O Gorukmez, O Gorukmez, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]|August 10, 2012
Cellular and molecular properties of (90)Y-labeled cetuximab in combination with radiotherapy on human tumor cells in vitroM Saki, M Toulany, W Sihver, et al.
Clinical Genetics|March 17, 2012
Clinical and molecular analysis of RASopathies in a group of Turkish patientsP Ö Şimşek-Kiper, Y Alanay, B Gülhan, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|August 30, 2012
Flow cytometric cell-based assay to preselect antibody constructs for radionuclide conjugationM Ingargiola, C Dittfeld, R Runge, et al.
Leukemia|March 16, 2007
Clonal duplication of a germline PTPN11 mutation due to acquired uniparental disomy in acute lymphoblastic leukemia blasts from a patient with Noonan syndromeA Karow, D Steinemann, G Göhring, et al.
Clinical Genetics|January 31, 2012
A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same familyW Y Ng, F Pasutto, T M Bardakjian, et al.
Experimental and Clinical Endocrinology & Diabetes : Official Journal, German Society of Endocrinology [And] German Diabetes Association|June 5, 2008
Infantile hypophosphatasia due to a new compound heterozygous TNSALP mutation - functional evidence for a hydrophobic side-chain?B Utsch, I Brun-Heath, G Staatz, et al.
American Journal of Human Genetics|October 16, 1999
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasiaI Quack, B Vonderstrass, M Stock, et al.
Kidney International|August 17, 2006
Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disordersK Hasselbacher, R C Wiggins, V Matejas, et al.
Pageof 6