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Laura K Conlin

Showing results (11-20 of 85) with videos related to

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International Journal of Molecular Sciences|May 4, 2026
Evaluation of PacBio Long-Read and PCR-Based Short-Read Sequencing for Mitochondrial DNA (mtDNA) Variant Detection, with an Emphasis on Detection and Quantification of mtDNA DeletionTanaya Jadhav, Matthew Aruta, Maria Alejandra Diaz-Miranda, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septumMoira A Crowley, Laura K Conlin, Elaine H Zackai, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotoniaAiko Iwata-Otsubo, Alyssa L Ritter, Brooke Weckselbatt, et al.
Nature Genetics|February 5, 2003
Natural variation in human gene expression assessed in lymphoblastoid cellsVivian G Cheung, Laura K Conlin, Teresa M Weber, et al.
Cancer Genetics|January 31, 2012
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemiaLinsheng Zhang, Iya Znoyko, Luciano J Costa, et al.
American Journal of Medical Genetics. Part A|July 23, 2015
Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepanciesMinjie Luo, Surabhi Mulchandani, Holly A Dubbs, et al.
Plos One|October 21, 2014
Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndromeManinder Kaur, Kosuke Izumi, Alisha B Wilkens, et al.
Molecular Cytogenetics|March 6, 2022
Characterization of a rare mosaic unbalanced translocation of t(3;12) in a patient with neurodevelopmental disordersXiaolin Hu, Elizabeth K Baker, Jodie Johnson, et al.
Molecular Cytogenetics|August 5, 2022
Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphismDong Li, Alanna Strong, Cuiping Hou, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Update on "two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20"Cheryl Descipio, Jennifer D Morrissette, Laura K Conlin, et al.
Pageof 9

Showing results (11-20 of 85) with videos related to

Sort By:
Pageof 9
International Journal of Molecular Sciences|May 4, 2026
Evaluation of PacBio Long-Read and PCR-Based Short-Read Sequencing for Mitochondrial DNA (mtDNA) Variant Detection, with an Emphasis on Detection and Quantification of mtDNA DeletionTanaya Jadhav, Matthew Aruta, Maria Alejandra Diaz-Miranda, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Further evidence for the possible role of MEIS2 in the development of cleft palate and cardiac septumMoira A Crowley, Laura K Conlin, Elaine H Zackai, et al.
American Journal of Medical Genetics. Part A|November 14, 2017
DOCK3-related neurodevelopmental syndrome: Biallelic intragenic deletion of DOCK3 in a boy with developmental delay and hypotoniaAiko Iwata-Otsubo, Alyssa L Ritter, Brooke Weckselbatt, et al.
Nature Genetics|February 5, 2003
Natural variation in human gene expression assessed in lymphoblastoid cellsVivian G Cheung, Laura K Conlin, Teresa M Weber, et al.
Cancer Genetics|January 31, 2012
Clonal diversity analysis using SNP microarray: a new prognostic tool for chronic lymphocytic leukemiaLinsheng Zhang, Iya Znoyko, Luciano J Costa, et al.
American Journal of Medical Genetics. Part A|July 23, 2015
Detection of mutually exclusive mosaicism in a girl with genotype-phenotype discrepanciesMinjie Luo, Surabhi Mulchandani, Holly A Dubbs, et al.
Plos One|October 21, 2014
Genome-wide expression analysis in fibroblast cell lines from probands with Pallister Killian syndromeManinder Kaur, Kosuke Izumi, Alisha B Wilkens, et al.
Molecular Cytogenetics|March 6, 2022
Characterization of a rare mosaic unbalanced translocation of t(3;12) in a patient with neurodevelopmental disordersXiaolin Hu, Elizabeth K Baker, Jodie Johnson, et al.
Molecular Cytogenetics|August 5, 2022
Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphismDong Li, Alanna Strong, Cuiping Hou, et al.
American Journal of Medical Genetics. Part A|May 27, 2010
Update on "two siblings with alternate unbalanced recombinants derived from a large cryptic maternal pericentric inversion of chromosome 20"Cheryl Descipio, Jennifer D Morrissette, Laura K Conlin, et al.
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