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1دورية أكاديمية
المؤلفون: B. F. Meyer, A. Buras, K. Gregor, L. S. Layritz, A. Principe, J. Kreyling, A. Rammig, C. S. Zang
المصدر: Biogeosciences, Vol 21, Pp 1355-1370 (2024)
وصف الملف: electronic resource
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2
المؤلفون: S M, Wakil, R, Ram, N P, Muiya, E, Andres, N, Mazhar, S, Hagos, M, Alshahid, B F, Meyer, G, Morahan, N, Dzimiri
المصدر: Clinical genetics. 90(6)
مصطلحات موضوعية: Male, Genotype, Genome, Human, Cholesterol, HDL, LIM Domain Proteins, Polymorphism, Single Nucleotide, Arabs, Cholesterol Ester Transfer Proteins, Phenotype, Humans, Female, Genetic Predisposition to Disease, Co-Repressor Proteins, Genome-Wide Association Study
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3
المؤلفون: D, Monies, N, Abu Al Saud, N, Sahar, B F, Meyer
المصدر: Animal genetics. 42(2)
مصطلحات موضوعية: Genetic Markers, Male, Gene Frequency, Genetic Loci, Animals, Female, Horses, Sequence Analysis, DNA, Multiplex Polymerase Chain Reaction, Microsatellite Repeats, Pedigree
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4
المؤلفون: H Nazer, H Banjar, M H Al-Hamed, B F Meyer, I Moggari, M Kambouris
المصدر: European Journal of Pediatrics. 159:303-309
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Cystic Fibrosis, Cystic Fibrosis Transmembrane Conductance Regulator, Heteroduplex Analysis, Biology, medicine.disease_cause, Polymerase Chain Reaction, Cystic fibrosis, Frameshift mutation, Exon, medicine, Humans, Point Mutation, Frameshift Mutation, ΔF508, Alleles, Genetics, Mutation, Splice site mutation, Point mutation, Exons, Sequence Analysis, DNA, medicine.disease, Cystic fibrosis transmembrane conductance regulator, Arabs, Pediatrics, Perinatology and Child Health, biology.protein
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5
المؤلفون: N. Sahar, D. Monies, B. F. Meyer, N. Abu Al Saud
المصدر: Animal Genetics. 42:225-226
مصطلحات موضوعية: education.field_of_study, Evolutionary biology, Population, Genetics, Microsatellite, Animal Science and Zoology, General Medicine, Biology, education
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6
المؤلفون: A al-Mehaidib, M Kambouris, I Mogarri, H Banjar, B F Meyer
المصدر: Annals of tropical paediatrics. 19(1)
مصطلحات موضوعية: Male, medicine.medical_specialty, Pancreatic disease, Cystic Fibrosis, 030231 tropical medicine, Population, Saudi Arabia, Cystic Fibrosis Transmembrane Conductance Regulator, Ethnic origin, medicine.disease_cause, Cystic fibrosis, Gastroenterology, 03 medical and health sciences, Exon, 0302 clinical medicine, 030225 pediatrics, Internal medicine, medicine, Humans, Nasal polyps, Allele, education, Mutation, education.field_of_study, business.industry, Infant, medicine.disease, Endocrinology, Child, Preschool, Pediatrics, Perinatology and Child Health, Exocrine Pancreatic Insufficiency, Female, business
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7
المؤلفون: E, Al-Jishi, B F, Meyer, M S, Rashed, M, Al-Essa, M H, Al-Hamed, N, Sakati, S, Sanjad, P T, Ozand, M, Kambouris
المصدر: Clinical genetics. 55(6)
مصطلحات موضوعية: Male, Reverse Transcriptase Polymerase Chain Reaction, Infant, Newborn, Humans, Infant, Point Mutation, Female, Genes, Recessive, Gas Chromatography-Mass Spectrometry, Gene Deletion, Glutathione Synthase
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8
المؤلفون: G A, Diaz, B D, Gelb, F, Ali, N, Sakati, S, Sanjad, B F, Meyer, M, Kambouris
المصدر: American journal of medical genetics. 85(1)
مصطلحات موضوعية: Genotype, Hypoparathyroidism, Developmental Disabilities, Chromosome Mapping, Genes, Recessive, Syndrome, Osteochondrodysplasias, Founder Effect, Phenotype, Haplotypes, Chromosomes, Human, Pair 1, Seizures, Intellectual Disability, Mutation, Humans, Abnormalities, Multiple, Child, Alleles
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9
المؤلفون: M H, Qari, S H, Khalil, M, Kambouris, B F, Meyer
المصدر: British journal of haematology. 103(2)
مصطلحات موضوعية: Cyclin-Dependent Kinase Inhibitor p21, Genes, p16, Nucleic Acid Heteroduplexes, DNA, Neoplasm, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Polymerase Chain Reaction, Cyclin-Dependent Kinases, Neoplasm Proteins, Cyclins, Mutation, Humans, Genes, Tumor Suppressor, Enzyme Inhibitors, Gene Deletion
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10
المؤلفون: A. Oldfors, H. Tajsharghi, L. E. Thornell, B. F. Meyer
المصدر: Neurology. 64:580-581
مصطلحات موضوعية: Neurology (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2fb03b35880c1d8bdfdb4fb66788a78f
https://doi.org/10.1212/wnl.64.3.580-a