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Friedel Wenzel

Showing results (21-30 of 25) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2006
Reliable detection of trisomy 21 using MALDI-TOF mass spectrometryDorothy J Huang, Matthew R Nelson, Bernhard Zimmermann, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: clinical and array-CGH study of a benign phenotype in a three-generation familyIsabel Filges, Benno Röthlisberger, Christoph Noppen, et al.
Current Oncology (Toronto, Ont.)|February 24, 2022
Co-Occurring CSF3R W791* Germline and Somatic T618I Driver Mutations Induce Early CNL and Clonal Progression to Mixed Phenotype Acute LeukemiaFranziska C Adam, Jakub Szybinski, Jörg P Halter, et al.
Cancer Research|October 26, 2013
3'-UTR poly(T/U) tract deletions and altered expression of EWSR1 are a hallmark of mismatch repair-deficient cancersShivendra Kishore, Salvatore Piscuoglio, Michal B Kovac, et al.
Gene|January 14, 2012
High resolution array in the clinical approach to chromosomal phenotypesIsabel Filges, Luzia Suda, Peter Weber, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 17, 2006
Reliable detection of trisomy 21 using MALDI-TOF mass spectrometryDorothy J Huang, Matthew R Nelson, Bernhard Zimmermann, et al.
American Journal of Medical Genetics. Part A|January 24, 2009
Familial 14.5 Mb interstitial deletion 13q21.1-13q21.33: clinical and array-CGH study of a benign phenotype in a three-generation familyIsabel Filges, Benno Röthlisberger, Christoph Noppen, et al.
Current Oncology (Toronto, Ont.)|February 24, 2022
Co-Occurring CSF3R W791* Germline and Somatic T618I Driver Mutations Induce Early CNL and Clonal Progression to Mixed Phenotype Acute LeukemiaFranziska C Adam, Jakub Szybinski, Jörg P Halter, et al.
Cancer Research|October 26, 2013
3'-UTR poly(T/U) tract deletions and altered expression of EWSR1 are a hallmark of mismatch repair-deficient cancersShivendra Kishore, Salvatore Piscuoglio, Michal B Kovac, et al.
Gene|January 14, 2012
High resolution array in the clinical approach to chromosomal phenotypesIsabel Filges, Luzia Suda, Peter Weber, et al.
Pageof 3