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Israel Gomy

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Familial Cancer|June 18, 2011
Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individualsMev Dominguez Valentin, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, et al.
Lancet Regional Health. Americas|March 11, 2026
Precision diagnosis and therapy for pediatric central nervous system tumors: consensus from the Brazilian Society of Pediatric Oncology (SOBOPE)Kevin Augusto Farias de Alvarenga, Juliana Oliveira de Araújo, Marina Rezende da Silveira, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 1, 2022
Identification and Management of Pathogenic Variants in BRCA1, BRCA2, and PALB2 in a Tumor-Only Genomic Testing ProgramBrittany L Bychkovsky, Tianyu Li, Jilliane Sotelo, et al.
Cancers|July 12, 2025
Advancing the Landscape of Clinical Actionability in Von Hippel-Lindau Syndrome: An Evidence-Based Framework from the INT<sup>2</sup>GRATE Oncology ConsortiumDiane R Koeller, McKenzie Walker, Busra Unal, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndromeRebecca L Hood, Matthew A Lines, Sarah M Nikkel, et al.
Cancers|December 10, 2021
Newborn Screening for the Detection of the <i>TP53</i> R337H Variant and Surveillance for Early Diagnosis of Pediatric Adrenocortical Tumors: Lessons Learned and Way ForwardKarina C F Tosin, Edith F Legal, Mara A D Pianovski, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Familial Cancer|June 18, 2011
Characterization of germline mutations of MLH1 and MSH2 in unrelated south American suspected Lynch syndrome individualsMev Dominguez Valentin, Felipe Carneiro da Silva, Erika Maria Monteiro dos Santos, et al.
Lancet Regional Health. Americas|March 11, 2026
Precision diagnosis and therapy for pediatric central nervous system tumors: consensus from the Brazilian Society of Pediatric Oncology (SOBOPE)Kevin Augusto Farias de Alvarenga, Juliana Oliveira de Araújo, Marina Rezende da Silveira, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 1, 2022
Identification and Management of Pathogenic Variants in BRCA1, BRCA2, and PALB2 in a Tumor-Only Genomic Testing ProgramBrittany L Bychkovsky, Tianyu Li, Jilliane Sotelo, et al.
Cancers|July 12, 2025
Advancing the Landscape of Clinical Actionability in Von Hippel-Lindau Syndrome: An Evidence-Based Framework from the INT<sup>2</sup>GRATE Oncology ConsortiumDiane R Koeller, McKenzie Walker, Busra Unal, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in SRCAP, encoding SNF2-related CREBBP activator protein, cause Floating-Harbor syndromeRebecca L Hood, Matthew A Lines, Sarah M Nikkel, et al.
Cancers|December 10, 2021
Newborn Screening for the Detection of the <i>TP53</i> R337H Variant and Surveillance for Early Diagnosis of Pediatric Adrenocortical Tumors: Lessons Learned and Way ForwardKarina C F Tosin, Edith F Legal, Mara A D Pianovski, et al.
Research Square|June 21, 2024
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseasesHellen Lesmann, Alexander Hustinx, Shahida Moosa, et al.
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