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Charis Eng

Showing results (381-390 of 555) with videos related to

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The New England Journal of Medicine|August 2, 2008
Multiple tumors in a child with germ-line mutations in TP53 and PTENSharon E Plon, Michael L Pirics, Jed Nuchtern, et al.
The New England Journal of Medicine|May 28, 2020
WWP1 Gain-of-Function Inactivation of PTEN in Cancer PredispositionYu-Ru Lee, Lamis Yehia, Takahiro Kishikawa, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 19, 2013
Increased prevalence of eosinophilic gastrointestinal disorders in pediatric PTEN hamartoma tumor syndromesCarol J Henderson, Joanne Ngeow, Margaret H Collins, et al.
American Journal of Human Genetics|November 3, 2015
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid CancerLamis Yehia, Farshad Niazi, Ying Ni, et al.
Proceedings. IEEE International Symposium on Biomedical Imaging|September 4, 2020
LEARNING TO DETECT BRAIN LESIONS FROM NOISY ANNOTATIONSDavood Karimi, Jurriaan M Peters, Abdelhakim Ouaalam, et al.
Molecular Autism|January 29, 2021
Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autismThomas W Frazier, Ritika Jaini, Robyn M Busch, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Unusual features in a patient with neurofibromatosis type 1: multiple subcutaneous lipomas, a juvenile polyp in ascending colon, congenital intrahepatic portosystemic venous shunt, and horseshoe kidneyCagatay Oktenli, Davut Gul, M Salih Deveci, et al.
Journal of Autism and Developmental Disorders|February 17, 2021
Brief Report: Role of Parent-Reported Executive Functioning and Anxiety in Insistence on Sameness in Individuals with Germline PTEN MutationsMirko Uljarević, Thomas W Frazier, Gaëlle Rached, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 13, 2013
Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical centerBrandie Heald, Thomas Plesec, Xiuli Liu, et al.
Plos One|April 18, 2023
Microbiomic profiles of bile in patients with benign and malignant pancreaticobiliary diseaseShyam K Poudel, Roshan Padmanabhan, Heloni Dave, et al.
Pageof 56

Showing results (381-390 of 555) with videos related to

Sort By:
Pageof 56
The New England Journal of Medicine|August 2, 2008
Multiple tumors in a child with germ-line mutations in TP53 and PTENSharon E Plon, Michael L Pirics, Jed Nuchtern, et al.
The New England Journal of Medicine|May 28, 2020
WWP1 Gain-of-Function Inactivation of PTEN in Cancer PredispositionYu-Ru Lee, Lamis Yehia, Takahiro Kishikawa, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 19, 2013
Increased prevalence of eosinophilic gastrointestinal disorders in pediatric PTEN hamartoma tumor syndromesCarol J Henderson, Joanne Ngeow, Margaret H Collins, et al.
American Journal of Human Genetics|November 3, 2015
Germline Heterozygous Variants in SEC23B Are Associated with Cowden Syndrome and Enriched in Apparently Sporadic Thyroid CancerLamis Yehia, Farshad Niazi, Ying Ni, et al.
Proceedings. IEEE International Symposium on Biomedical Imaging|September 4, 2020
LEARNING TO DETECT BRAIN LESIONS FROM NOISY ANNOTATIONSDavood Karimi, Jurriaan M Peters, Abdelhakim Ouaalam, et al.
Molecular Autism|January 29, 2021
Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autismThomas W Frazier, Ritika Jaini, Robyn M Busch, et al.
American Journal of Medical Genetics. Part A|May 20, 2004
Unusual features in a patient with neurofibromatosis type 1: multiple subcutaneous lipomas, a juvenile polyp in ascending colon, congenital intrahepatic portosystemic venous shunt, and horseshoe kidneyCagatay Oktenli, Davut Gul, M Salih Deveci, et al.
Journal of Autism and Developmental Disorders|February 17, 2021
Brief Report: Role of Parent-Reported Executive Functioning and Anxiety in Insistence on Sameness in Individuals with Germline PTEN MutationsMirko Uljarević, Thomas W Frazier, Gaëlle Rached, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 13, 2013
Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical centerBrandie Heald, Thomas Plesec, Xiuli Liu, et al.
Plos One|April 18, 2023
Microbiomic profiles of bile in patients with benign and malignant pancreaticobiliary diseaseShyam K Poudel, Roshan Padmanabhan, Heloni Dave, et al.
Pageof 56