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European Journal of Medical Genetics|August 19, 2019
Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypesStephanie Q Zhang, Julie Fleischer, Hussam Al-Kateb, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists|February 9, 2017
Association of Li-Fraumeni Syndrome With Small Cell Carcinoma of the Ovary, Hypercalcemic Type and Concurrent Pleomorphic Liposarcoma of the CervixBevan Tandon, Ian S Hagemann, Horacio M Maluf, et al.
Head and Neck Pathology|July 14, 2026
Biphenotypic Sinonasal Sarcomas with Recurrent PAX3::FOXO6 Gene FusionRumeal D Whaley, Antonina A Wojcik, Hussam Al-Kateb, et al.
American Journal of Medical Genetics. Part A|November 26, 2010
Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomaliesHussam Al-Kateb, Amanda Hahn, Julie M Gastier-Foster, et al.
Cancer Genetics|April 19, 2018
Unexpected favorable outcome in a patient with high grade B-cell lymphoma with abnormalities of MYC, BCL6 and BCL2 lociThomas Adams, Deborah Fuchs, Patricia K Shadoan, et al.
European Journal of Human Genetics : EJHG|April 22, 2004
Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemiaJohannes Dietter, Alexander Spiegel, Dieter an Mey, 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.
International Journal of Surgical Pathology|May 21, 2024
NTRK3-Rearranged Prostatic Acinar Adenocarcinoma: Report of a Patient and Review of the LiteratureRumeal D Whaley, Burak Tekin, Michael R McCarthy, et al.
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