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Joseph Shen

Showing results (1-10 of 19) with videos related to

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Clinical Orthopaedics and Related Research|February 12, 2008
Type III acetabular defect revision with bilobed components: five-year resultsJoseph T Moskal, Michael E Higgins, Joseph Shen
Cureus|September 9, 2025
Superior Mesenteric Artery Syndrome: A Case ReportJoseph Shen, Kevin Shen, Brandon Weissman, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
Scoliosis and vertebral anomalies: additional abnormal phenotypes associated with chromosome 16p11.2 rearrangementHussam Al-Kateb, Geetika Khanna, Isabel Filges, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2009
Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspectsAyman W El-Hattab, Fang-Yuan Li, Joseph Shen, et al.
Radiology|August 20, 2004
Improvement in radiologists' characterization of malignant and benign breast masses on serial mammograms with computer-aided diagnosis: an ROC studyLubomir Hadjiiski, Heang-Ping Chan, Berkman Sahiner, et al.
Radiology|June 28, 2006
Breast masses: computer-aided diagnosis with serial mammogramsLubomir Hadjiiski, Berkman Sahiner, Mark A Helvie, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Joseph Shen, et al.
Genes, Chromosomes & Cancer|November 7, 2015
An infant with MLH3 variants, FOXG1-duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing studyRina Kansal, Xinmin Li, Joseph Shen, et al.
Clinical Genetics|October 30, 2025
Expansion of the Phenotypic and Genotypic Spectrum for PRKAR1B-Related Marbach-Schaaf Neurodevelopmental Syndrome: A Case SeriesSebastian Burkart, Tarik Guzeloglu, Ana R Soares, et al.
Nature Genetics|November 25, 2014
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Clinical Orthopaedics and Related Research|February 12, 2008
Type III acetabular defect revision with bilobed components: five-year resultsJoseph T Moskal, Michael E Higgins, Joseph Shen
Cureus|September 9, 2025
Superior Mesenteric Artery Syndrome: A Case ReportJoseph Shen, Kevin Shen, Brandon Weissman, et al.
American Journal of Medical Genetics. Part A|January 25, 2014
Scoliosis and vertebral anomalies: additional abnormal phenotypes associated with chromosome 16p11.2 rearrangementHussam Al-Kateb, Geetika Khanna, Isabel Filges, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 23, 2009
Maternal systemic primary carnitine deficiency uncovered by newborn screening: clinical, biochemical, and molecular aspectsAyman W El-Hattab, Fang-Yuan Li, Joseph Shen, et al.
Radiology|August 20, 2004
Improvement in radiologists' characterization of malignant and benign breast masses on serial mammograms with computer-aided diagnosis: an ROC studyLubomir Hadjiiski, Heang-Ping Chan, Berkman Sahiner, et al.
Radiology|June 28, 2006
Breast masses: computer-aided diagnosis with serial mammogramsLubomir Hadjiiski, Berkman Sahiner, Mark A Helvie, et al.
European Journal of Human Genetics : EJHG|October 22, 2009
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Joseph Shen, et al.
Genes, Chromosomes & Cancer|November 7, 2015
An infant with MLH3 variants, FOXG1-duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing studyRina Kansal, Xinmin Li, Joseph Shen, et al.
Clinical Genetics|October 30, 2025
Expansion of the Phenotypic and Genotypic Spectrum for PRKAR1B-Related Marbach-Schaaf Neurodevelopmental Syndrome: A Case SeriesSebastian Burkart, Tarik Guzeloglu, Ana R Soares, et al.
Nature Genetics|November 25, 2014
Mutations in the voltage-gated potassium channel gene KCNH1 cause Temple-Baraitser syndrome and epilepsyCas Simons, Lachlan D Rash, Joanna Crawford, et al.
Pageof 2