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Kristin Cabral

Showing results (1-10 of 7) with videos related to

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Nature Methods|March 16, 2010
Identifying single-cell molecular programs by stochastic profilingKevin A Janes, Chun-Chao Wang, Karin J Holmberg, et al.
Bone|April 14, 2023
X-linked hypophosphatemia in 4 generations due to an exon 13-15 duplication in PHEX, in the absence of the c.*231A>G variantJulio Soto Barros, Sabrina I Sanchez, Kristin Cabral, et al.
BMC Medical Genetics|November 15, 2018
De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case reportChrystal F Mavros, Catherine A Brownstein, Roshni Thyagrajan, et al.
Blood Advances|February 27, 2025
Integrative cytogenetic and molecular studies unmask "chromosomal mimicry" in hematologic malignanciesMelissa Zhao, Scott Ryall, Samuel J Brody, et al.
The American Journal of Psychiatry|August 24, 2022
Similar Rates of Deleterious Copy Number Variants in Early-Onset Psychosis and Autism Spectrum DisorderCatherine A Brownstein, Elise Douard, Josephine Mollon, et al.
Molecular Psychiatry|February 18, 2021
RCL1 copy number variants are associated with a range of neuropsychiatric phenotypesCatherine A Brownstein, Richard S Smith, Lance H Rodan, et al.
Advanced Genetics (Hoboken, N.J.)|December 31, 2025
Rare Structural Variants Uncovered by Optical Genome Mapping in Multisystem Inflammatory Syndrome in Children (MIS-C)Catherine A Brownstein, Caspar I van der Made, Kristin Cabral, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Nature Methods|March 16, 2010
Identifying single-cell molecular programs by stochastic profilingKevin A Janes, Chun-Chao Wang, Karin J Holmberg, et al.
Bone|April 14, 2023
X-linked hypophosphatemia in 4 generations due to an exon 13-15 duplication in PHEX, in the absence of the c.*231A>G variantJulio Soto Barros, Sabrina I Sanchez, Kristin Cabral, et al.
BMC Medical Genetics|November 15, 2018
De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case reportChrystal F Mavros, Catherine A Brownstein, Roshni Thyagrajan, et al.
Blood Advances|February 27, 2025
Integrative cytogenetic and molecular studies unmask "chromosomal mimicry" in hematologic malignanciesMelissa Zhao, Scott Ryall, Samuel J Brody, et al.
The American Journal of Psychiatry|August 24, 2022
Similar Rates of Deleterious Copy Number Variants in Early-Onset Psychosis and Autism Spectrum DisorderCatherine A Brownstein, Elise Douard, Josephine Mollon, et al.
Molecular Psychiatry|February 18, 2021
RCL1 copy number variants are associated with a range of neuropsychiatric phenotypesCatherine A Brownstein, Richard S Smith, Lance H Rodan, et al.
Advanced Genetics (Hoboken, N.J.)|December 31, 2025
Rare Structural Variants Uncovered by Optical Genome Mapping in Multisystem Inflammatory Syndrome in Children (MIS-C)Catherine A Brownstein, Caspar I van der Made, Kristin Cabral, et al.
Pageof 1