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Malik Alawi

Showing results (11-20 of 130) with videos related to

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Blood|April 23, 2014
Next-generation sequencing of peripheral B-lineage cells pinpoints the circulating clonotypic cell pool in multiple myelomaBenjamin Thiele, Marie Kloster, Malik Alawi, et al.
Pediatric Blood & Cancer|March 24, 2016
Rapid Capture Next-Generation Sequencing in Clinical Diagnostics of Kinase Pathway Aberrations in B-Cell Precursor ALLUdo Zur Stadt, Gabriele Escherich, Daniela Indenbirken, et al.
Plos Pathogens|July 29, 2015
A Comprehensive Analysis of Replicating Merkel Cell Polyomavirus Genomes Delineates the Viral Transcription Program and Suggests a Role for mcv-miR-M1 in Episomal PersistenceJuliane Marie Theiss, Thomas Günther, Malik Alawi, et al.
Pediatrics|December 30, 2016
Acute Liver Failure Meets SOPH Syndrome: A Case Report on an Intermediate PhenotypeFanny Kortüm, Iris Marquardt, Malik Alawi, et al.
Emerging Infectious Diseases|June 18, 2016
Pegivirus Infection in Domestic Pigs, GermanyChristine Baechlein, Adam Grundhoff, Nicole Fischer, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Elsahy-Waters syndrome is caused by biallelic mutations in CDH11Frederike L Harms, Sheela Nampoothiri, Shams Anazi, et al.
Scientific Reports|June 18, 2017
Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sampleThomas Günther, Ludwig Haas, Malik Alawi, et al.
European Journal of Human Genetics : EJHG|May 1, 2014
An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndromeHengameh Abdollahpour, Malik Alawi, Fanny Kortüm, et al.
European Journal of Haematology|December 19, 2015
Correlation of somatic mutations with outcome after FLAMSA-busulfan sequential conditioning and allogeneic stem cell transplantation in patients with myelodysplastic syndromesMaximilian Christopeit, Anita Badbaran, Malik Alawi, et al.
European Journal of Human Genetics : EJHG|December 17, 2015
A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B geneKatta Mohan Girisha, Fanny Kortüm, Hitesh Shah, et al.
Pageof 13

Showing results (11-20 of 130) with videos related to

Sort By:
Pageof 13
Blood|April 23, 2014
Next-generation sequencing of peripheral B-lineage cells pinpoints the circulating clonotypic cell pool in multiple myelomaBenjamin Thiele, Marie Kloster, Malik Alawi, et al.
Pediatric Blood & Cancer|March 24, 2016
Rapid Capture Next-Generation Sequencing in Clinical Diagnostics of Kinase Pathway Aberrations in B-Cell Precursor ALLUdo Zur Stadt, Gabriele Escherich, Daniela Indenbirken, et al.
Plos Pathogens|July 29, 2015
A Comprehensive Analysis of Replicating Merkel Cell Polyomavirus Genomes Delineates the Viral Transcription Program and Suggests a Role for mcv-miR-M1 in Episomal PersistenceJuliane Marie Theiss, Thomas Günther, Malik Alawi, et al.
Pediatrics|December 30, 2016
Acute Liver Failure Meets SOPH Syndrome: A Case Report on an Intermediate PhenotypeFanny Kortüm, Iris Marquardt, Malik Alawi, et al.
Emerging Infectious Diseases|June 18, 2016
Pegivirus Infection in Domestic Pigs, GermanyChristine Baechlein, Adam Grundhoff, Nicole Fischer, et al.
American Journal of Medical Genetics. Part A|December 23, 2017
Elsahy-Waters syndrome is caused by biallelic mutations in CDH11Frederike L Harms, Sheela Nampoothiri, Shams Anazi, et al.
Scientific Reports|June 18, 2017
Recovery of the first full-length genome sequence of a parapoxvirus directly from a clinical sampleThomas Günther, Ludwig Haas, Malik Alawi, et al.
European Journal of Human Genetics : EJHG|May 1, 2014
An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndromeHengameh Abdollahpour, Malik Alawi, Fanny Kortüm, et al.
European Journal of Haematology|December 19, 2015
Correlation of somatic mutations with outcome after FLAMSA-busulfan sequential conditioning and allogeneic stem cell transplantation in patients with myelodysplastic syndromesMaximilian Christopeit, Anita Badbaran, Malik Alawi, et al.
European Journal of Human Genetics : EJHG|December 17, 2015
A novel multiple joint dislocation syndrome associated with a homozygous nonsense variant in the EXOC6B geneKatta Mohan Girisha, Fanny Kortüm, Hitesh Shah, et al.
Pageof 13