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Jeanne Meck

Showing results (1-10 of 11) with videos related to

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Journal of Cutaneous Pathology|September 3, 2011
Histiocytic sarcoma transdifferentiated from follicular lymphoma presenting as a cutaneous tumorWeifen Zeng, Jeanne Meck, Bruce D Cheson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2012
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexityKavita S Reddy, Swaroop Aradhya, Jeanne Meck, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndromeMohamed Khalifa, Jennifer Stein, Lance Grau, et al.
Molecular Vision|April 4, 2008
Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]Emre Zafer, Jeanne Meck, Liora Gerrad, et al.
American Journal of Medical Genetics. Part A|January 22, 2004
Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalitiesSaid Baidas, T-J Chen, Valentin Kolev, et al.
American Journal of Hematology|November 26, 2002
CD5-negative, CD10-negative small B-cell leukemia: variant of chronic lymphocytic leukemia or a distinct entity?Salwa S Sheikh, Bhaskar V S Kallakury, Khawla A Al-Kuraya, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2021
Uniparental disomy in a population of 32,067 clinical exome triosJulie Scuffins, Jennifer Keller-Ramey, Lindsay Dyer, et al.
European Journal of Medical Genetics|April 27, 2018
Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumorsJohn C Herriges, Sara Brown, Maria Longhurst, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohortKyle Retterer, Julie Scuffins, Daniel Schmidt, et al.
Human Mutation|August 11, 2018
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVarErin R Riggs, Tristan Nelson, Andrew Merz, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Cutaneous Pathology|September 3, 2011
Histiocytic sarcoma transdifferentiated from follicular lymphoma presenting as a cutaneous tumorWeifen Zeng, Jeanne Meck, Bruce D Cheson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 1, 2012
A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexityKavita S Reddy, Swaroop Aradhya, Jeanne Meck, et al.
American Journal of Medical Genetics. Part A|March 16, 2013
Partial deletion of ANKRD11 results in the KBG phenotype distinct from the 16q24.3 microdeletion syndromeMohamed Khalifa, Jennifer Stein, Lance Grau, et al.
Molecular Vision|April 4, 2008
Autosomal dominant congenital cataract in a Libyan Jewish family: cosegregation with a reciprocal chromosomal translocation [t(3;5)(p22.3; p15.1)]Emre Zafer, Jeanne Meck, Liora Gerrad, et al.
American Journal of Medical Genetics. Part A|January 22, 2004
Constitutional trisomy 8 mosaicism due to meiosis II non-disjunction in a phenotypically normal woman with hematologic abnormalitiesSaid Baidas, T-J Chen, Valentin Kolev, et al.
American Journal of Hematology|November 26, 2002
CD5-negative, CD10-negative small B-cell leukemia: variant of chronic lymphocytic leukemia or a distinct entity?Salwa S Sheikh, Bhaskar V S Kallakury, Khawla A Al-Kuraya, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 26, 2021
Uniparental disomy in a population of 32,067 clinical exome triosJulie Scuffins, Jennifer Keller-Ramey, Lindsay Dyer, et al.
European Journal of Medical Genetics|April 27, 2018
Identification of two 14q32 deletions involving DICER1 associated with the development of DICER1-related tumorsJohn C Herriges, Sara Brown, Maria Longhurst, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 31, 2014
Assessing copy number from exome sequencing and exome array CGH based on CNV spectrum in a large clinical cohortKyle Retterer, Julie Scuffins, Daniel Schmidt, et al.
Human Mutation|August 11, 2018
Copy number variant discrepancy resolution using the ClinGen dosage sensitivity map results in updated clinical interpretations in ClinVarErin R Riggs, Tristan Nelson, Andrew Merz, et al.
Pageof 2