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Trilochan Sahoo

Showing results (11-20 of 65) with videos related to

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Prenatal Diagnosis|January 10, 2018
ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?Sara B Hay, Trilochan Sahoo, Mary K Travis, et al.
Molecular Cytogenetics|May 3, 2012
BCR-JAK2 fusion as a result of a translocation (9;22)(p24;q11.2) in a patient with CML-like myeloproliferative diseaseMohamed M Elnaggar, Sally Agersborg, Trilochan Sahoo, et al.
Molecular Cytogenetics|July 10, 2012
Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomaliesDaniel L Di Bartolo, Mohamed El Naggar, Renius Owen, et al.
American Journal of Medical Genetics. Part A|June 19, 2008
15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridizationNicola Brunetti-Pierri, Trilochan Sahoo, Sarah Frioux, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndromeRichard J Schroer, Arthur L Beaudet, Marwan Shinawi, et al.
Reproductive Biomedicine Online|May 6, 2022
The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriagesJenna Finley, Sara Hay, Jeannine Oldzej, et al.
American Journal of Medical Genetics. Part A|November 15, 2005
Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangementsTrilochan Sahoo, Chad A Shaw, Andrew S Young, et al.
European Journal of Human Genetics : EJHG|November 3, 2011
Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypesSoo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, et al.
Annals of Neurology|March 24, 2005
Creatine metabolism in combined methylmalonic aciduria and homocystinuriaOlaf A Bodamer, Trilochan Sahoo, Arthur L Beaudet, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotypeJia-Chi Wang, Mary Vaccarello-Cruz, Leslie Ross, et al.
Pageof 7

Showing results (11-20 of 65) with videos related to

Sort By:
Pageof 7
Prenatal Diagnosis|January 10, 2018
ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?Sara B Hay, Trilochan Sahoo, Mary K Travis, et al.
Molecular Cytogenetics|May 3, 2012
BCR-JAK2 fusion as a result of a translocation (9;22)(p24;q11.2) in a patient with CML-like myeloproliferative diseaseMohamed M Elnaggar, Sally Agersborg, Trilochan Sahoo, et al.
Molecular Cytogenetics|July 10, 2012
Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomaliesDaniel L Di Bartolo, Mohamed El Naggar, Renius Owen, et al.
American Journal of Medical Genetics. Part A|June 19, 2008
15q13q14 deletions: phenotypic characterization and molecular delineation by comparative genomic hybridizationNicola Brunetti-Pierri, Trilochan Sahoo, Sarah Frioux, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndromeRichard J Schroer, Arthur L Beaudet, Marwan Shinawi, et al.
Reproductive Biomedicine Online|May 6, 2022
The genomic basis of sporadic and recurrent pregnancy loss: a comprehensive in-depth analysis of 24,900 miscarriagesJenna Finley, Sara Hay, Jeannine Oldzej, et al.
American Journal of Medical Genetics. Part A|November 15, 2005
Array-based comparative genomic hybridization analysis of recurrent chromosome 15q rearrangementsTrilochan Sahoo, Chad A Shaw, Andrew S Young, et al.
European Journal of Human Genetics : EJHG|November 3, 2011
Unique and atypical deletions in Prader-Willi syndrome reveal distinct phenotypesSoo-Jeong Kim, Jennifer L Miller, Paul J Kuipers, et al.
Annals of Neurology|March 24, 2005
Creatine metabolism in combined methylmalonic aciduria and homocystinuriaOlaf A Bodamer, Trilochan Sahoo, Arthur L Beaudet, et al.
American Journal of Medical Genetics. Part A|May 21, 2013
Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotypeJia-Chi Wang, Mary Vaccarello-Cruz, Leslie Ross, et al.
Pageof 7