المؤلفون: Naoya Kitamura, Yuki Ito, Tomoko Kawai, Hiromi Kamura, Michihiro Yamamura, Haruna Okubo, Akihiro Hasegawa, Momoko Inoue, Ken Takahashi, Michiko Miya, Hiroshi Kawame, Osamu Samura, Aikou Okamoto

المصدر: Taiwanese Journal of Obstetrics & Gynecology, Vol 63, Iss 3, Pp 418-421 (2024)

مصطلحات موضوعية: Chromosomes, Human, Pair 6, Mosaicism, Uniparental disomy, DNA methylation, Gynecology and obstetrics, RG1-991

وصف الملف: electronic resource

العلاقة: http://www.sciencedirect.com/science/article/pii/S102845592400086XTest; https://doaj.org/toc/1028-4559Test

الوصول الحر: https://doaj.org/article/ad813741264b4cc3964235c9e890d556Test

المؤلفون: Zerka Rashid, Veerendra Babu, Shyam Sundar Sharma, Pradeep Kumar Singh, Sudha Krishnan Nair

المصدر: Theoretical and Applied Genetics. 135:4549-4563

مصطلحات موضوعية: Plant Breeding, Fusarium, Genetics, Humans, Chromosomes, Human, Pair 6, General Medicine, Zea mays, Polymorphism, Single Nucleotide, Agronomy and Crop Science, Disease Resistance, Genome-Wide Association Study, Plant Diseases, Biotechnology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d227135d2cd4e11f918593e0c2a0dab8Test
https://doi.org/10.1007/s00122-022-04239-0Test

المؤلفون: Valentina A. Zavala, Sandro Casavilca-Zambrano, Jeannie Navarro-Vásquez, Carlos A. Castañeda, Guillermo Valencia, Zaida Morante, Monica Calderón, Julio E. Abugattas, Henry Gómez, Hugo A. Fuentes, Ruddy Liendo-Picoaga, Jose M. Cotrina, Claudia Monge, Silvia P. Neciosup, Scott Huntsman, Donglei Hu, Sixto E. Sánchez, Michelle A. Williams, Angel Núñez-Marrero, Lenin Godoy, Aaron Hechmer, Adam B. Olshen, Julie Dutil, Elad Ziv, Jovanny Zabaleta, Bizu Gelaye, Jule Vásquez, Marco Gálvez-Nino, Daniel Enriquez-Vera, Tatiana Vidaurre, Laura Fejerman

المصدر: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, vol 31, iss 8

مصطلحات موضوعية: Receptor, ErbB-2, Epidemiology, Breast Neoplasms, Medical and Health Sciences, Chromosomes, ErbB-2, Receptors, Breast Cancer, Peru, Genetics, 2.1 Biological and endogenous factors, Humans, Aetiology, Progesterone, Cancer, Hispanic or Latino, Estrogen, Good Health and Well Being, Logistic Models, Receptors, Estrogen, Oncology, Chromosomes, Human, Pair 6, Female, Pair 6, Receptors, Progesterone, Human, Receptor

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0bd86dc0c3582edc36da5f555c29ec8Test
https://doi.org/10.1158/1055-9965.epi-22-0069Test

المؤلفون: Alexandra E. Kovach, Elena Zerkalenkova, Ludmila Zemtsova, Aleksandra Borkovskaya, Marina Gaskova, Marat Kazanov, Alexander Popov, Liudmila Baidun, Michael Maschan, Alexey Maschan, Paul S. Gaynon, Deepa Bhojwani, Galina Novichkova, Yulia Olshanskaya, Gordana Raca

المصدر: Cancer Genetics. :37-40

مصطلحات موضوعية: Chromosomes, Human, X, Cancer Research, Oncogene Proteins, Fusion, Sequence Analysis, RNA, Infant, Translocation, Genetic, Leukemia, Myeloid, Acute, Proto-Oncogene Proteins c-myb, Genetics, Humans, Chromosomes, Human, Pair 6, Female, GATA1 Transcription Factor, Chromosomes, Human, Pair 9, Molecular Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::956e41fd4fe42a6ab5e11239967ca34bTest
https://doi.org/10.1016/j.cancergen.2021.11.007Test

المؤلفون: Aafke Engwerda, Maarten P. van den Berg, Wilhelmina S. Kerstjens-Frederikse, Yvonne J. Vos, Bert B.A. de Vries, Tuula Rinne, Marc T R Roofthooft, Paulien A Terhal, Patrick Deelen, Conny M. A. van Ravenswaaij-Arts, Barbara Frentz, Katharina Löhner, Trijnie Dijkhuizen, Erika Leenders

المساهمون: Cardiovascular Centre (CVC), Clinical Cognitive Neuropsychiatry Research Program (CCNP)

المصدر: European Journal of Human Genetics, 29, 1669-1676. Nature Publishing Group
Eur J Hum Genet

مصطلحات موضوعية: Joint Instability, CONGENITAL HEART-DEFECTS, Pathology, medicine.medical_specialty, TAK1, Heart Valve Diseases, Cardiomyopathy, GROWTH FAILURE, Dwarfism, Disease, Short stature, Article, Mitral valve, Genetics, medicine, Humans, MICRODELETION, DYSPLASIA, Genetics (clinical), Exome sequencing, Adaptor Proteins, Signal Transducing, business.industry, Syndrome, medicine.disease, Phenotype, DELINEATION, medicine.anatomical_structure, Mitral Valve, Noonan syndrome, Chromosomes, Human, Pair 6, medicine.symptom, Cardiomyopathies, Haploinsufficiency, business, Gene Deletion

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd540b65f880419358b12d518f7ffd4Test
https://doi.org/10.1038/s41431-021-00948-0Test

المؤلفون: Hongmei Zhang, Kaishan Tao, Xu Guo, Yang Liu, Zhenyuan Bian, Kaixiang Zhou, Dongnan Guo, Yang Wang, Lin Wang, Xiangxu Wang, Xiwen Gu, Liping Su, Kun Liu, Jinliang Xing

المصدر: Cancer Science

مصطلحات موضوعية: Genetic Markers, Male, Genetics, Genomics and Proteomics, Oncology, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, medicine.medical_specialty, Carcinoma, Hepatocellular, DNA Copy Number Variations, endocrine system diseases, Prognostic prediction, Kaplan-Meier Estimate, Free dna, Disease-Free Survival, Internal medicine, mental disorders, Biomarkers, Tumor, medicine, Humans, Copy-number variation, cell‐free DNA, Noninvasive biomarkers, Prediction score, Framingham Risk Score, Whole Genome Sequencing, business.industry, Liver Neoplasms, biomarkers, DNA, Neoplasm, Original Articles, hepatocellular carcinoma, General Medicine, Middle Aged, Prognosis, medicine.disease, Treatment Outcome, copy number variations, Cell-free fetal DNA, Hepatocellular carcinoma, Chromosomes, Human, Pair 6, Female, Original Article, Chromosomes, Human, Pair 4, business, Cell-Free Nucleic Acids, Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 17, Chromosomes, Human, Pair 8

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24b804650f57fadf5acdd97e3ee33ccTest
https://doi.org/10.1111/cas.15128Test

المؤلفون: Gang Zheng, Qi Shen, Wei Wang, Lina Shao, Lan Zheng, Ji Yuan, Young L. Kim, Guillermo Garcia-Manero, Yongzhong Yuan, Xiaohui Zhang, Xiaojun Wu, Rong He, L. Jeffrey Medeiros, Yulei Shen, Hong Fang, Sunyi Chi, Mariko Yabe, Sanam Loghavi, Shimin Hu, Peng Wei, Dong Chen, Guiling Tang

المصدر: Modern Pathology. 34:1143-1152

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Oncology, medicine.medical_specialty, Pathology, Myeloid, Adolescent, Oncogene Proteins, Fusion, Chromosomal Proteins, Non-Histone, medicine.medical_treatment, Hematopoietic stem cell transplantation, Translocation, Genetic, Pathology and Forensic Medicine, Young Adult, 03 medical and health sciences, 0302 clinical medicine, hemic and lymphatic diseases, Internal medicine, White blood cell, medicine, Humans, Oncogene Fusion, Child, Poly-ADP-Ribose Binding Proteins, Survival analysis, Aged, Aged, 80 and over, Oncogene Proteins, business.industry, Myeloid leukemia, Middle Aged, medicine.disease, Nuclear Pore Complex Proteins, Transplantation, Leukemia, Myeloid, Acute, stomatognathic diseases, 030104 developmental biology, medicine.anatomical_structure, Basophilia, Myelodysplastic Syndromes, 030220 oncology & carcinogenesis, Chromosomes, Human, Pair 6, Female, Bone marrow, Chromosomes, Human, Pair 9, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc9af5aa9e8126928422b4d02980a464Test
https://doi.org/10.1038/s41379-021-00741-wTest

المؤلفون: Hreinn Stefansson, Esben Agerbo, Konstantinos Kamperis, Ole Mors, Viðar Örn Eðvarðsson, Thomas Werge, Ditte Demontis, Jane H. Christensen, Veera M. Rajagopal, Mette Nyegaard, Merete Nordentoft, Jakob Grove, Thomas Damm Als, Preben Bo Mortensen, Anders D. Børglum, Henriette Thisted Horsdal, Cecilie Siggaard Jørgensen, G. Bragi Walters, Kari Stefansson, David M. Hougaard, Søren Rittig

المصدر: Jørgensen, C S, Horsdal, H T, Rajagopal, V M, Grove, J, Als, T D, Kamperis, K, Nyegaard, M, Walters, G B, Eðvarðsson, V Ö, Stefánsson, H, Nordentoft, M, Hougaard, D M, Werge, T, Mors, O, Mortensen, P B, Agerbo, E, Rittig, S, Stefánsson, K, Børglum, A D, Demontis, D & Christensen, J H 2021, ' Identification of genetic loci associated with nocturnal enuresis : a genome-wide association study ', The Lancet Child and Adolescent Health, vol. 5, no. 3, pp. 201-209 . https://doi.org/10.1016/S2352-4642Test(20)30350-3

مصطلحات موضوعية: Male, Autism Spectrum Disorder, Genome-wide association study, Nocturnal, 03 medical and health sciences, 0302 clinical medicine, Enuresis, 030225 pediatrics, Developmental and Educational Psychology, medicine, Humans, Deamino Arginine Vasopressin, 030212 general & internal medicine, Child, Desmopressin, Chromosome 13, Genetics, Chromosomes, Human, Pair 13, business.industry, Genetic Variation, medicine.disease, Genetic architecture, Phenotype, Attention Deficit Disorder with Hyperactivity, Genetic Loci, Autism spectrum disorder, Pediatrics, Perinatology and Child Health, Cohort, Chromosomes, Human, Pair 6, Female, medicine.symptom, business, Genome-Wide Association Study, Nocturnal Enuresis, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::489d4081140e133353f9a91e999e2b55Test
https://doi.org/10.1016/s2352-4642Test(20)30350-3

المؤلفون: Mian-Ling Zhong, Ye-Mei Song, Chao-Chun Zou

المصدر: JCRPE, Vol 13, Iss 1, Pp 109-113 (2021)
Journal of Clinical Research in Pediatric Endocrinology

مصطلحات موضوعية: China, Pediatrics, medicine.medical_specialty, Microcephaly, Language delay, Endocrinology, Diabetes and Metabolism, media_common.quotation_subject, growth retardation, Case Report, 6q25 microdeletion, lcsh:Diseases of the endocrine glands. Clinical endocrinology, Craniofacial Abnormalities, Facial dysmorphism, Endocrinology, Intellectual disability, medicine, Humans, Language Development Disorders, Girl, Growth Disorders, language delay, media_common, Low-set ears, lcsh:RC648-665, Growth retardation, business.industry, lcsh:RJ1-570, lcsh:Pediatrics, facial dysmorphism, medicine.disease, intellectual disability, Child, Preschool, Pediatrics, Perinatology and Child Health, Chromosomes, Human, Pair 6, Female, Chromosome Deletion, Differential diagnosis, medicine.symptom, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2af693f22a95c625cccdf55d12b29aadTest
https://doi.org/10.4274/jcrpe.galenos.2020.2020.0008Test

المؤلفون: Langxin Chen, Guiying Zhang, Qifu Li, Rong Lin

المصدر: Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. 28

مصطلحات موضوعية: China, Risk Factors, Incidence, Humans, Chromosomes, Human, Pair 6, Genetic Predisposition to Disease, Hematology, General Medicine, Polymorphism, Single Nucleotide, Ischemic Stroke

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e2c2a22a586fa306ffcabcf0c5a889bTest
https://pubmed.ncbi.nlm.nih.gov/35188813Test