المؤلفون: Paul T. Finch, Christine C. Odom, Wayne L. Furman, Eniko K. Pivnick

المصدر: American Journal of Medical Genetics Part A. 155:1162-1164

مصطلحات موضوعية: Male, Oncology, medicine.medical_specialty, business.industry, Chromosomes, Human, Pair 22, Cancer, 22q11 2 microdeletion, Wilms' tumor, Microdeletion syndrome, medicine.disease, Wilms Tumor, Endocrinology, Child, Preschool, DiGeorge syndrome, Immunopathology, Internal medicine, Genetics, Humans, Medicine, In patient, Chromosome Deletion, business, Genetics (clinical), Kidney disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2570a7d7a5f011858d70fdcf66e6102c
https://doi.org/10.1002/ajmg.a.33957

المؤلفون: Christine C. Odom, Charles G. Mullighan, Kim E. Nichols, James R. Downing, Rose B. McGee, Joy Nakitandwe, Jinjun Cheng, Panduka Nagahawatte, Xiaotu Ma, Li Dong, Tanja A. Gruber, Matthew Parker, Jared Becksfort, Amanda Larson Gedman, Ching-Hon Pui, Robert Huether, Amar Gajjar, Alberto S. Pappo, Michael Rusch, David W. Ellison, Bhavin Vadodaria, Sheila A. Shurtleff, Richard K. Wilson, Erin Hedlund, John Easton, Gang Wu, Jinjun Dang, Gordon Lemmon, Zachary J Faber, Jinghui Zhang, Michael N. Edmonson, Elaine R. Mardis, Xiang Chen, Michael Walsh, Donald Yergeau

المصدر: Blood. 124:127-127

مصطلحات موضوعية: Childhood leukemia, Immunology, Cancer, Cell Biology, Hematology, Biology, Bioinformatics, medicine.disease_cause, medicine.disease, Biochemistry, Pediatric cancer, Leukemia, Germline mutation, MUTYH, medicine, Cancer research, KRAS, Carcinogenesis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::df6ff02ef380adf7297ef2b5a4aea2b9
https://doi.org/10.1182/blood.v124.21.127.127

المؤلفون: Huddleston S; The Hamilton Eye Institute, Department of Ophthalmology, University of Tennessee Health Science Center, Memphis, Tennessee 38163, USA., McNall-Knapp RY, Siatkowski M, Odom C, Brennan R, Wilson MW

المصدر: Ophthalmic genetics [Ophthalmic Genet] 2013 Mar-Jun; Vol. 34 (1-2), pp. 97-100. Date of Electronic Publication: 2012 Aug 27.

نوع المنشور: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 9436057 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1744-5094 (Electronic) Linking ISSN: 13816810 NLM ISO Abbreviation: Ophthalmic Genet Subsets: MEDLINE

مواضيع طبية MeSH: Translocation, Genetic*, Brain Neoplasms/*genetics , Chromosomes, Human, Pair 11/*genetics , Chromosomes, Human, Pair 13/*genetics , Neuroectodermal Tumors, Primitive/*genetics , Retinal Neoplasms/*genetics , Retinoblastoma/*genetics, Brain Neoplasms/pathology ; Brain Neoplasms/therapy ; Child ; Combined Modality Therapy ; Female ; Germ-Line Mutation ; Humans ; In Situ Hybridization, Fluorescence ; Karyotyping ; Magnetic Resonance Imaging ; Neuroectodermal Tumors, Primitive/pathology ; Neuroectodermal Tumors, Primitive/therapy ; Retinal Neoplasms/diagnosis ; Retinoblastoma/diagnosis ; Retinoblastoma Protein/genetics