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المؤلفون: Amandine Moriot, Diana Hall
المصدر: Genetics in medicine, vol. 21, no. 3, pp. 613-621
مصطلحات موضوعية: Forensic Genetics, Genetic Markers, 0301 basic medicine, Genotype, Population, 030105 genetics & heredity, Biology, Fathers, 03 medical and health sciences, chemistry.chemical_compound, Fetus, Gene Frequency, INDEL Mutation, Pregnancy, Prenatal Diagnosis, Humans, Alleles, Biomarkers/blood, Cell-Free Nucleic Acids/analysis, Cell-Free Nucleic Acids/genetics, DNA/blood, Female, Forensic Genetics/methods, Gene Frequency/genetics, Genetic Markers/genetics, INDEL Mutation/genetics, Microsatellite Repeats/genetics, Paternal Inheritance/genetics, Polymorphism, Genetic/genetics, Prenatal Diagnosis/methods, Sequence Analysis, DNA/methods, Cell-free DNA, DIP-STR, DNA mixture, Noninvasive prenatal testing, Paternity testing, Allele, education, Genetics (clinical), Genetics, education.field_of_study, Polymorphism, Genetic, DNA, Sequence Analysis, DNA, 030104 developmental biology, chemistry, Cell-free fetal DNA, Genetic marker, Paternal Inheritance, Microsatellite, Cell-Free Nucleic Acids, Biomarkers, Microsatellite Repeats
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::881d9d5cf98ce01f846a1bf22d129e30Test
https://doi.org/10.1038/s41436-018-0102-9Test -
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المؤلفون: Sergey Nikolaev, Armand Bottani, Stylianos E. Antonarakis, Daniel Robyr, Federico Santoni, Michel Guipponi, Periklis Makrythanasis
المصدر: Genome Res, vol. 24, no. 2, pp. 349-55
Genome Research
Genome Research, Vol. 24, No 2 (2014) pp. 349-55مصطلحات موضوعية: medicine.medical_specialty, Genotype, Population, Single-nucleotide polymorphism, Biology, Compound heterozygosity, Polymorphism, Single Nucleotide, Algorithms, Computational Biology/methods, Databases, Genetic, Gene Frequency, Genetic Predisposition to Disease, Humans, INDEL Mutation/*genetics, Phenotype, Polymorphism, Single Nucleotide/*genetics, Sequence Analysis, DNA, Software, symbols.namesake, INDEL Mutation, Genetics, medicine, ddc:576.5, Allele, Indel, education, Genetics (clinical), education.field_of_study, Computational Biology, 3. Good health, Mendelian inheritance, symbols, Medical genetics
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::421fa6bcb7ac36d4d0736e816be65fb6Test
https://serval.unil.ch/notice/serval:BIB_F69325586088Test -
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المؤلفون: Ceylan Ayada, Ümran Toru, Sebahat Turgut, Osman Genç, Günfer Turgut, Server Sahin, A. Yerlikaya
مصطلحات موضوعية: Gene Frequency, Genetic Association Studies, Genetic Predisposition to Disease, Humans, INDEL Mutation/*genetics, Peptidyl-Dipeptidase A/*genetics, Pulmonary Disease, Chronic Obstructive/*genetics/pathology, Renin-Angiotensin System/*genetics, Risk Factors, Turkey, genomic DNA, genetic association, genotype, polymerase chain reaction, genetic risk, Gastroenterology, Turkey (republic), Turkish population, Renin-Angiotensin System, Pulmonary Disease, Chronic Obstructive, INDEL Mutation, renin angiotensin aldosterone system, Genotype, genetic variability, genetic polymorphism, genetics, pathophysiology, COPD, education.field_of_study, clinical article, biology, Chronic obstructive pulmonary disease, allele, General Medicine, risk factor, Renin angiotensin system, blood sampling, Angiotensin converting enzyme, medicine.medical_specialty, Population, dipeptidyl carboxypeptidase, DNA determination, Peptidyl-Dipeptidase A, Article, Internal medicine, geographic distribution, medicine, Genetic predisposition, ACE protein, human, heterozygosity, controlled study, human, education, Molecular Biology, Allele frequency, gene identification, business.industry, population genetics, Angiotensin-converting enzyme, ACE gene, medicine.disease, DNA isolation, Endocrinology, gene function, biology.protein, gene expression, Turk (people), pathology, homozygosity, business, genetic predisposition, chronic obstructive lung disease, Blood sampling
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f6d6032137ce50699698c4d9415dcd5Test
https://hdl.handle.net/20.500.12438/4548Test