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Thomas Liehr

Showing results (71-80 of 586) with videos related to

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Journal of Mother and Child|July 19, 2022
Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndromeEmir Behluli, Nexhibe Nuhii, Thomas Liehr, et al.
Cytogenetic and Genome Research|April 22, 2021
PrefaceVladimir A Trifonov, Marcelo B Cioffi, Thomas Liehr
Molecular Cytogenetics|July 24, 2015
Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocationFrenny Sheth, Thomas Liehr, Krati Shah, et al.
International Journal of Molecular Sciences|September 28, 2023
The Diagnostic, Prognostic, and Therapeutic Potential of Cell-Free DNA with a Special Focus on COVID-19 and Other Viral InfectionsGalina Hovhannisyan, Tigran Harutyunyan, Rouben Aroutiounian, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 1, 2005
Increased efficiency of fluorescence in situ hybridization (FISH) using the microwaveAnja Weise, Thomas Liehr, Uwe Claussen, et al.
Oncology Letters|February 15, 2014
<i>De novo</i> acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case reportWalid Al Achkar, Abdulmunim Aljapawe, Thomas Liehr, et al.
Oncology Letters|June 14, 2013
Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate-resistant chronic myeloid leukemia patientWalid Al-Achkar, Abdulsamad Wafa, Adnan Ikhtiar, et al.
Oncology Letters|July 31, 2012
A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemiaWalid Al-Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Oncology Letters|July 12, 2012
A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12)Walid Al-Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Human Genome Variation|October 23, 2024
Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring systemSílvia Pires, Paula Jorge, Thomas Liehr, et al.
Pageof 59

Showing results (71-80 of 586) with videos related to

Sort By:
Pageof 59
Journal of Mother and Child|July 19, 2022
Suspicions regarding the genetic inheritance of acute lymphoblastic leukemia in patients with down syndromeEmir Behluli, Nexhibe Nuhii, Thomas Liehr, et al.
Cytogenetic and Genome Research|April 22, 2021
PrefaceVladimir A Trifonov, Marcelo B Cioffi, Thomas Liehr
Molecular Cytogenetics|July 24, 2015
Prader-Willi syndrome - type 1 deletion, a consequence of an unbalanced translocation of chromosomes 13 and 15, easily to be mixed up with a Robertsonian translocationFrenny Sheth, Thomas Liehr, Krati Shah, et al.
International Journal of Molecular Sciences|September 28, 2023
The Diagnostic, Prognostic, and Therapeutic Potential of Cell-Free DNA with a Special Focus on COVID-19 and Other Viral InfectionsGalina Hovhannisyan, Tigran Harutyunyan, Rouben Aroutiounian, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|June 1, 2005
Increased efficiency of fluorescence in situ hybridization (FISH) using the microwaveAnja Weise, Thomas Liehr, Uwe Claussen, et al.
Oncology Letters|February 15, 2014
<i>De novo</i> acute myeloid leukemia subtype-M4 with initial trisomy 8 and later acquired t(3;12)(q26;p12) leading to ETV6/MDS1/EVI1 fusion transcript expression: A case reportWalid Al Achkar, Abdulmunim Aljapawe, Thomas Liehr, et al.
Oncology Letters|June 14, 2013
Three-way Philadelphia translocation t(9;10;22)(q34;p11.2;q11.2) as a secondary abnormality in an imatinib mesylate-resistant chronic myeloid leukemia patientWalid Al-Achkar, Abdulsamad Wafa, Adnan Ikhtiar, et al.
Oncology Letters|July 31, 2012
A unique cytogenetic abnormality, t(2;7)(p13.1;p21.3), in a Philadelphia-positive chronic myeloid leukemiaWalid Al-Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Oncology Letters|July 12, 2012
A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12)Walid Al-Achkar, Abdulsamad Wafa, Faten Moassass, et al.
Human Genome Variation|October 23, 2024
Challenges in classifying human chromosomal heteromorphisms using banding cytogenetics: From controversial guidelines to the need for a universal scoring systemSílvia Pires, Paula Jorge, Thomas Liehr, et al.
Pageof 59