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1دورية أكاديمية
المؤلفون: Marta Olszewska, Ewa Wiland, Nataliya Huleyuk, Monika Fraczek, Alina T. Midro, Danuta Zastavna, Maciej Kurpisz
المصدر: BMC Medical Genomics, Vol 12, Iss 1, Pp 1-19 (2019)
مصطلحات موضوعية: Chromosome topology, Familial translocation, Nuclear architecture, Reciprocal chromosome translocation, Sperm chromosomes, Male infertility, Internal medicine, RC31-1245, Genetics, QH426-470
وصف الملف: electronic resource
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2دورية أكاديمية
المؤلفون: Olszewska, MartaAff1, Wiland, EwaAff1, Huleyuk, NataliyaAff2, Fraczek, MonikaAff1, Midro, Alina T.Aff3, Zastavna, DanutaAff2, Aff4, Kurpisz, MaciejAff1
المصدر: BMC Medical Genomics. 12(1)
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3دورية أكاديمية
المؤلفون: Midro, Alina T., Zollino, Marcella, Wiland, Ewa, Panasiuk, Barbara, Iwanowski, Piotr S., Murdolo, Marina, Śmigiel, Robert, Sąsiadek, Maria, Pilch, Jacek, Kurpisz, Maciej
المصدر: Journal of Assisted Reproduction and Genetics: An Official Journal of the American Society for Reproductive Medicine. February 2016 33(2):189-197
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4كتاب إلكتروني
المؤلفون: Connelly, M. A.Aff15, Grady, R. C.Aff15, Mushinski, J. F.Aff15, Aff16, Marcu, K. B.Aff15
المساهمون: Capron, A., editorAff1, Compans, R. W., editorAff2, Cooper, M., editorAff2, Koprowski, H., editorAff3, McConnell, I., editorAff4, Melchers, F., editorAff5, Oldstone, M., editorAff6, Olsnes, S., editorAff7, Potter, M., editorAff8, Saedler, H., editorAff9, Vogt, P. K., editorAff10, Wagner, H., editorAff11, Wilson, I., editorAff12, Potter, Michael, editorAff13, Melchers, Fritz, editorAff14
المصدر: Mechanisms in B-Cell Neoplasia 1992 : Workshop at the National Cancer Institute, National Institutes of Health, Bethesda, MD, USA, April 21–23, 1992. 182:229-236
Degree: M. D
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5كتاب
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المؤلفون: Jacek Pilch, Maria Sąsiadek, Piotr S. Iwanowski, Marcella Zollino, Alina T. Midro, Maciej Kurpisz, Ewa Wiland, Barbara Panasiuk, Marina Murdolo, Robert Śmigiel
المصدر: Journal of Assisted Reproduction and Genetics
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Heterozygote, Chromosome Breakpoints, Genetic Counseling, Trisomy, 030105 genetics & heredity, Biology, Settore MED/03 - GENETICA MEDICA, Translocation, Genetic, Chromosome segregation, 03 medical and health sciences, 0302 clinical medicine, Meiosis, Chromosome Segregation, Obstetrics and Gynaecology, medicine, Genetics, Humans, Genetics(clinical), Wolf–Hirschhorn syndrome, Genetics (clinical), Meiotic segregation pattern, In Situ Hybridization, Fluorescence, 030219 obstetrics & reproductive medicine, Wolf-Hirschhorn Syndrome, Breakpoint, Obstetrics and Gynecology, Karyotype, General Medicine, medicine.disease, Chromosome translocations, Spermatozoa, Pedigree, FISH mapping, Reproductive Medicine, Karyotyping, Female, Reciprocal chromosome translocation, Chromosomes, Human, Pair 4, Pedigree segregation analysis, Developmental Biology
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7كتاب إلكتروني
المؤلفون: Johnstone, Alan P.Aff4
المساهمون: Althaus, Felix R., editorAff1, Hilz, Helmuth, editorAff2, Shall, Sydney, editorAff3
المصدر: ADP-Ribosylation of Proteins. :424-428
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8دورية أكاديمية
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تسجيل الدخول للوصول الكامل. -
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المؤلفون: Tahsin Yakut, Yalçın Kimya, Sebnem Ozemri Sag, Mutlu Karkucak
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Genetik Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Kadın Hastalıkları ve Doğum Anabilim Dalı., Karkucak, Mutlu, Sağ, Şebnem Özemri, Yakut, Tahsin, Kimya, Yalçın, AAH-8355-2021
مصطلحات موضوعية: Breakpoints, Male, Trisomy 21, Cell division, Karyometry, Prenatal diagnosis, Aneuploidy, Chromosomal translocation, X chromosome, Chromosome translocation 12, Genetics (clinical), Risk assessment, Genetics, Karyotype 47,XXX, Sperm FISH, Fluorescence in situ hybridization, Genetics & heredity, Chromosome 18, In-sıtu hybridization, Chromosome 13, Chromosome 21, Female, Reciprocal chromosome translocation, Chromosome 21q, Human, Adult, Rearrangements, Genetic counseling, Translocation, Constitutional, Chromosome G band, Biology, Article, Chromosome polymorphism, Case report, Genetic screening, medicine, Chromosome translocation 1, Chromosomal-aberrations, Genetic risk, Y chromosome, Fish analysis, Wolf-Hirschhorn Syndrome, Phenotype, EF Hand Motif, medicine.disease, Sperm, Amniocentesis, Genetic association, Semen analysis, Carriers, Chromosome 11p, Fragile sites, Trisomy
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8414336993c08c056f6d461a4d27d904
http://hdl.handle.net/11452/24978 -
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المؤلفون: Ugur Ozbek, Leyla Agaoglu, Sema Anak, Inci Yildiz, Omer Devecioglu, Sema Sirma, Cetin Timur, Adalet Meral, Gunduz Gedikoglu, Lebriz Yüksel
المساهمون: Uludağ Üniversitesi/Tıp Fakültesi/Çocuk Sağlığı ve Hastalıkları Anabilim Dalı., Meral, Adalet, U-6138-2017, C-9513-2017
المصدر: Journal of pediatric hematology/oncology. 25(3)
مصطلحات موضوعية: Oncology, Male, Pathology, Unclassified drug, Oncogene Proteins, Fusion, Turkey, TEL-AML1, Cryptic t(12-21), Hybrid protein, Chromosomal translocation, Childhood leukemia, Acute lymphoblastic leukemia, Pediatrics, Fusion gene, Acute Lymphoblastic Leukemia, Chromosome 21, Pre B Lymphocyte, Turkey (republic), hemic and lymphatic diseases, Pediatric leukemia, Relapse, Child, Children, Priority journal, Hematology, Incidence (epidemiology), Precursor Cell Lymphoblastic Leukemia-Lymphoma, Transcript, Prognosis, Reverse transcription polymerase chain reaction, Survival Rate, Child, Preschool, Core Binding Factor Alpha 2 Subunit, Female, Reciprocal chromosome translocation, Human, medicine.medical_specialty, Adolescent, Major clinical study, Article, Immunophenotyping, Acute lymphocytic leukemia, Internal medicine, Tel aml1 protein, medicine, Humans, neoplasms, business.industry, Infant, Newborn, Infant, Pre b lymphocyte, Frequency, medicine.disease, Childhood, Fusion protein, Subgroup, Clinical feature, Fusion transcript, Pediatrics, Perinatology and Child Health, Kaplan meier method, Leukemia, lymphocytic, acute, business, TEL/AML1 fusion, Cancer incidence
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d5b2022e23daaa34e9a3aadafec85188
https://pubmed.ncbi.nlm.nih.gov/12621238