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Rachel D Burnside

Showing results (1-10 of 21) with videos related to

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Cytogenetic and Genome Research|August 18, 2015
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated FeaturesRachel D Burnside
Prenatal Diagnosis|January 24, 2019
Are all chromosome microarrays the same? What clinicians need to knowBrynn Levy, Rachel D Burnside
Genes|August 28, 2025
Optical Genome Mapping: A New Tool for Cytogenomic AnalysisBrynn Levy, Rachel D Burnside, Yassmine Akkari
Genes|April 26, 2025
Systemic EBV+ T-Cell Lymphoma of Childhood with Hemophagocytic Lymphohistiocytosis in a Patient with a Highly Complex KaryotypePatrick Maher, Emilia Guzman, Joanna Chaffin, et al.
Annals of Hematology|December 31, 2024
Severe aplastic anemia with acquired X chromosome clonality as a sole abnormalityTim Jang, Rachel D Burnside, Joanna Chaffin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2025
Reconciling competencies in undergraduate medical genetics education: APHMG versus PCME competenciesRachel D Burnside, Megan Boothe, David H Ledbetter, et al.
Cancer Genetics|February 27, 2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusionsPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
Pediatrics|May 29, 2013
Complex chromosome rearrangement of 6p25.3->p23 and 12q24.32->qter in a child with moyamoyaRebecca E Rosenberg, Maureen Egan, Shaun Rodgers, et al.
Cytogenetic and Genome Research|November 9, 2016
Constitutional Chromoanagenesis of Distal 13q in a Young Adult with Recurrent StrokesRachel D Burnside, April Harris, Darrow Speyer, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delayKrishna Yelavarthi, Huong Cabral, Golder N Wilson, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Cytogenetic and Genome Research|August 18, 2015
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated FeaturesRachel D Burnside
Prenatal Diagnosis|January 24, 2019
Are all chromosome microarrays the same? What clinicians need to knowBrynn Levy, Rachel D Burnside
Genes|August 28, 2025
Optical Genome Mapping: A New Tool for Cytogenomic AnalysisBrynn Levy, Rachel D Burnside, Yassmine Akkari
Genes|April 26, 2025
Systemic EBV+ T-Cell Lymphoma of Childhood with Hemophagocytic Lymphohistiocytosis in a Patient with a Highly Complex KaryotypePatrick Maher, Emilia Guzman, Joanna Chaffin, et al.
Annals of Hematology|December 31, 2024
Severe aplastic anemia with acquired X chromosome clonality as a sole abnormalityTim Jang, Rachel D Burnside, Joanna Chaffin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 28, 2025
Reconciling competencies in undergraduate medical genetics education: APHMG versus PCME competenciesRachel D Burnside, Megan Boothe, David H Ledbetter, et al.
Cancer Genetics|February 27, 2019
Multidisciplinary analysis of pediatric T-ALL: 9q34 gene fusionsPeter Papenhausen, Carla A Kelly, Zhenxi Zhang, et al.
Pediatrics|May 29, 2013
Complex chromosome rearrangement of 6p25.3->p23 and 12q24.32->qter in a child with moyamoyaRebecca E Rosenberg, Maureen Egan, Shaun Rodgers, et al.
Cytogenetic and Genome Research|November 9, 2016
Constitutional Chromoanagenesis of Distal 13q in a Young Adult with Recurrent StrokesRachel D Burnside, April Harris, Darrow Speyer, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delayKrishna Yelavarthi, Huong Cabral, Golder N Wilson, et al.
Pageof 3