المؤلفون: Anthoni, Heidi

مصطلحات موضوعية: Dyslexia -- genetics, Genetic predisposition to disease, Chromosome mapping, Chromosomes, human, pair 2 -- genetics, Chromosomes, human, pair 6 -- genetics, Translocation, genetic, Dyslexi, Genetik

Degree: Diss. (sammanfattning) Stockholm : Karolinska institutet, 2007

المؤلفون: Nathalie Besuchet Schmutz, Stylianos E. Antonarakis, Frédérique Béna, Danielle Martinet, Marie-Claude Addor, Armand Bottani, Sophie Dahoun, Jacques S. Beckmann, Isabel Filges, Michael A. Morris, Gaide Ac

المصدر: American Journal of Medical Genetics. A, Vol. 146A, No 16 (2008) pp. 2094-2102

مصطلحات موضوعية: Male, Genotype, Developmental Disabilities, Biology, Craniofacial Abnormalities, Gene mapping, Intellectual Disability, Gene duplication, Genetics, medicine, Humans, Abnormalities, Multiple, In Situ Hybridization, Fluorescence, Genetics (clinical), Oligonucleotide Array Sequence Analysis, ddc:616, Chromosomes, Human, Pair 6/ genetics, Corectopia, Infant, Chromosome, medicine.disease, Subtelomere, Hypsarrhythmia, Craniofacial Abnormalities/ genetics, Developmental disorder, Phenotype, Abnormalities, Multiple/ genetics, Child, Preschool, Karyotyping, Chromosome Inversion, Chromosomes, Human, Pair 6, Female, Mental Retardation/ genetics, Chromosome Deletion, medicine.symptom, Developmental Disabilities/ genetics, Comparative genomic hybridization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fe5c871d454b1545f025a352023c34b
https://doi.org/10.1002/ajmg.a.32414

المؤلفون: Shau Yin Ha, Rever Chak-ho Li, Hong-Yuan Luo, Hui Leung Yuen, Richard Sherva, Martin H. Steinberg, Paola Sebastiani, John J. Farrell, David H.K. Chui, Chi Keung Li, Zhi-yi Chen, Li Chong Chan, Lindsay A. Farrer, Acw Lee, Clinton T. Baldwin, Benjamin F. Chu, Chi Kong Li, Vivian Chan, Edmond S. K. Ma, Jason C. C. So

مصطلحات موضوعية: Adult, Male, Heterozygote, Linkage disequilibrium, Genes, myb, DNA Mutational Analysis, Molecular Sequence Data, Quantitative Trait Loci, Immunology, Population, Gene Expression, Single-nucleotide polymorphism, Genome-wide association study, Biology, Polymorphism, Single Nucleotide, Biochemistry, HBG2, Linkage Disequilibrium, Cohort Studies, Red Cells, Iron, and Erythropoiesis, Asian People, hemic and lymphatic diseases, Humans, education, Gene, Fetal Hemoglobin, DNA Primers, Sequence Deletion, Genetics, education.field_of_study, Base Sequence, beta-Thalassemia, Chromosome, Cell Biology, Hematology, Molecular biology, Fetal Hemoglobin - genetics, DNA binding site, Enhancer Elements, Genetic, Asian Continental Ancestry Group - genetics, Hong Kong, Chromosomes, Human, Pair 6, DNA, Intergenic, Female, K562 Cells, Chromosomes, Human, Pair 6 - genetics, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::747aa9966dc8b2619bb3ea9b5232dafd
http://hdl.handle.net/10722/139942

المؤلفون: Ya Lan Shieh, Brian E. Henderson, Pei Ei Wu, Jiajun Shi, Kelvin Y.K. Chan, Zhibin Hu, Wei Zheng, Bo Huang, Christopher A. Haiman, Guoliang Li, Loic Le Marchand, Martha J. Shrubsole, Regina M. Santella, Kexin Chen, Kazuo Tajima, William J. Blot, Keitaro Matsuo, Yu-Tang Gao, Lina Zhang, Sum Yin Chan, Chun Li, Marilie D. Gammon, Hongbing Shen, Kathleen M. Egan, Jirong Long, Amy Trentham-Dietz, Sandra L. Deming, Wei Lu, Hong Zheng, Ui-Soon Khoo, Shimian Qu, Yong Cui, Yoshio Kasuga, Wanqing Wen, Shoichiro Tsugane, Xiao-Ou Shu, Montserrat Garcia-Closas, Hiroji Iwata, Linda Titus-Ernstoff, Polly A. Newcomb, Alecia M. Fair, Furu Wang, Motoki Iwasaki, Chen-Yang Shen, Qiuyin Cai, Yong-Bing Xiang, Lisa B. Signorello

مصطلحات موضوعية: Oncology, Cancer Research, medicine.medical_specialty, Genotype, Genome-wide association study, Single-nucleotide polymorphism, Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, White People, Article, Breast cancer, Asian People, Polymorphism (computer science), Internal medicine, medicine, SNP, Humans, Genetic Predisposition to Disease, Allele, Genetics, Carcinoma, Case-control study, Genomics, Carcinoma - epidemiology - ethnology - genetics, Middle Aged, medicine.disease, Breast Neoplasms - epidemiology - ethnology - genetics, European Continental Ancestry Group - genetics, Asian Continental Ancestry Group - genetics, Case-Control Studies, Chromosomes, Human, Pair 6, Female, Chromosomes, Human, Pair 6 - genetics, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27d3871edae5473ae9a707c61ffcc868
http://hdl.handle.net/10722/137635

المؤلفون: Yan Li, Li Fu, Alissa Michelle Go Wong, Yan-Hui Fan, Miao-Xin Li, Jin-Xin Bei, Wei-Hua Jia, Yi-Xin Zeng, Danny Chan, Kenneth M C Cheung, Pak Sham, Daniel Chua, Xin-Yuan Guan, You-Qiang Song

المصدر: PLoS ONE
PLoS ONE, Vol 6, Iss 1, p e14562 (2011)

مصطلحات موضوعية: China, China - epidemiology, Science, Nasopharyngeal neoplasm, Single-nucleotide polymorphism, Human leukocyte antigen, Biology, Allelic Imbalance, Polymorphism, Single Nucleotide, law.invention, law, medicine, Humans, Genetic Predisposition to Disease, GABBR1, Genetics and Genomics/Cancer Genetics, Polymerase chain reaction, Adaptor Proteins, Signal Transducing, Nasopharyngeal Neoplasms - genetics, Genetics, Multidisciplinary, Oncology/Head and Neck Cancers, Haplotype, Nasopharyngeal Neoplasms, Genetics and Genomics/Gene Expression, medicine.disease, Phosphoproteins, Molecular biology, Gene Expression Regulation, Neoplastic, Nasopharyngeal carcinoma, Receptors, GABA-B, Case-Control Studies, Medicine, Chromosomes, Human, Pair 6, Chromosomes, Human, Pair 6 - genetics, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b398f532ac65813d069d4a8ffa9c1aa
https://pubmed.ncbi.nlm.nih.gov/21283797

المؤلفون: Stefania Gimelli, Ariane Paoloni-Giacobino, Frédérique Béna, James Lespinasse, François Ansermet

المصدر: Journal of Child Sexual Abuse, Vol. 19, No 3 (2010) pp. 337-344

مصطلحات موضوعية: Proband, Child abuse, Chromosomes, Human, Pair 6/*genetics, Domestic Violence, Genetic Carrier Screening, Poison control, Social Environment, Craniofacial Abnormalities, ddc:616.89, Domestic Violence/psychology, Pregnancy, Intellectual disability, ddc:576.5, Inbreeding, Intercellular Signaling Peptides and Proteins/*genetics, media_common, Genetics, Daughter, Chromosome Deletion, Child Abuse, Sexual/*psychology, Pedigree, Psychiatry and Mental health, Clinical Psychology, Phenotype, Intercellular Signaling Peptides and Proteins, Incest/*psychology, Chromosomes, Human, Pair 6, Female, Adult, medicine.medical_specialty, Adolescent, media_common.quotation_subject, Consanguinity, Father-Child Relations, Heterozygote Detection, Pathology and Forensic Medicine, Intellectual Disability, medicine, Humans, Psychiatry, business.industry, Child Abuse, Sexual, medicine.disease, Self Concept, Sexual abuse, Incest, Pediatrics, Perinatology and Child Health, business, Craniofacial Abnormalities/genetics/psychology, Intellectual Disability/*genetics/*psychology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::233916a0b68cf65680cf71ecb85a6d13
https://pubmed.ncbi.nlm.nih.gov/20509080

المؤلفون: Patsopoulos, N. A., Ioannidis, J. P.

مصطلحات موضوعية: Genetic Markers, Polymorphism, Genetic, Arthritis, Rheumatoid/*genetics/immunology, Peptides, Cyclic/genetics, Chromosomes, Human, Pair 6/*genetics/immunology, Genetic Loci, Complement C5/genetics, Rheumatoid Factor/genetics/immunology, Chromosome Mapping, Humans, Genetic Predisposition to Disease, TNF Receptor-Associated Factor 1/*genetics/immunology, Epidemiologic Methods

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_____10561::0d1e13283553538ebed099607b390844
http://olympias.lib.uoi.gr/jspui/handle/123456789/24781

المؤلفون: Semerci CN, Cinbis M, Ullmann R, Steininger A, Bahce M, Yagci B, Ozden S, Sabir N, Gumus D, Tepeli E, Arteaga J, Mutchinick OM

مصطلحات موضوعية: Adult, Child, Child, Preschool, Chromosomes, Human, Pair 12/*genetics, Chromosomes, Human, Pair 6/*genetics, Chromosomes, Human, X/*genetics, Comparative Genomic Hybridization, Female, Humans, In Situ Hybridization, Fluorescence, Infant, Newborn, Karyotyping, Male, Monosomy/*genetics, Phenotype, Pregnancy, Syndrome, Telomere/*genetics, Translocation, Genetic, Trisomy/*genetics, Young Adult

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3566::91761fb6857c318e0c3d400c8d9a3203

المؤلفون: Saitoh, Y., Bruner, J. M., Levin, V. A., Kyritsis, A. P.

مصطلحات موضوعية: Cyclin-Dependent Kinase Inhibitor p21, Genetic Markers, Alleles, Chromosomes, Human, Pair 6/*genetics, Humans, Astrocytoma/*genetics, Polymerase Chain Reaction/*methods, Chromosome Deletion, Exons, Glioma/genetics, Cyclins/genetics, Microsatellite Repeats

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od_____10561::868943e970d8f6294fd78ced045ca71f
http://olympias.lib.uoi.gr/jspui/handle/123456789/21060

المؤلفون: Najib Al-Khaja, Uppala Radhakrishna, Mohammed Naveed, Uppala Ratnamala, Jeffrey Golla, David Hutchings, Swapan K. Nath, Stylianos E. Antonarakis, Armand Bottani, Samuel Deutsch, Mathew Gaines, Mahmoud Taleb Al-Ali

المصدر: American Journal of Human Genetics, Vol. 80, No 1 (2007) pp. 105-111

مصطلحات موضوعية: Male, Foot Deformities, Congenital, Locus (genetics), Biology, Article, Gene mapping, Genetic linkage, Hand Deformities, Congenital/ genetics, Genetics, Genetic predisposition, Humans, Genetics(clinical), Genetics (clinical), ddc:616, Chromosomes, Human, Pair 6/ genetics, Genome, Human, Haplotype, Autosomal dominant trait, Chromosome Mapping, Foot Deformities, Congenital/ genetics, Chromosomes, Human, Pair 1/ genetics, Penetrance, Arabs, Pedigree, Haplotypes, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 6, Female, Disease Susceptibility, Hand Deformities, Congenital, SNP array

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db5659a891be6434c450b0bb4baec775