المؤلفون: L. Saksova, J. Gecz, L. Kadasl, V. Ferak

المصدر: Disease Markers, Vol 11, Iss 2-3, Pp 139-141 (1993)

مصطلحات موضوعية: Medicine (General), R5-920

Relation: http://dx.doi.org/10.1155/1993/791651; https://doaj.org/toc/0278-0240; https://doaj.org/toc/1875-8630; https://doaj.org/article/a091643281c14d44bec72d0def5917c8

الاتاحة: https://doi.org/10.1155/1993/791651
https://doaj.org/article/a091643281c14d44bec72d0def5917c8

المؤلفون: I, Zmetáková, V, Ferák, G, Minárik, A, Ficek, H, Poláková, E, Feráková, L, Kádasi

المصدر: General physiology and biophysics. 26(4)

مصطلحات موضوعية: Adult, Male, Slovakia, Roma, Adolescent, Siblings, Infant, Newborn, Bilirubin, Sequence Analysis, DNA, Consanguinity, Humans, Female, Glucuronosyltransferase, Child, Kernicterus, Gene Deletion, Crigler-Najjar Syndrome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::1564df1799c394c801cb0d47a3f271db
https://pubmed.ncbi.nlm.nih.gov/18281749

المؤلفون: L. Kadasi, J. Gecz, J. Matusek, T. Krivusova, V. Ferak, J. Hruskovic, G. Romeo, DEVOTO, MARCELLA

المساهمون: L., Kadasi, J., Gecz, J., Matusek, T., Krivusova, V., Ferak, Devoto, Marcella, J., Hruskovic, G., Romeo

Relation: info:eu-repo/semantics/altIdentifier/pmid/1376297; volume:89; issue:3; journal:HUMAN GENETICS; http://hdl.handle.net/11573/497417

الاتاحة: http://hdl.handle.net/11573/497417

المؤلفون: G, Minárik, V, Ferák, E, Feráková, A, Ficek, H, Poláková, L, Kádasi

المصدر: General physiology and biophysics. 22(4)

مصطلحات موضوعية: Male, Slovakia, Roma, Hearing Loss, Sensorineural, Syndrome, Connexins, Connexin 26, Child, Preschool, Mutation, Humans, Female, Genetic Predisposition to Disease, Child, Genes, Dominant

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::dbcde577f660124c2e1e42394c998677
https://pubmed.ncbi.nlm.nih.gov/15113126

المؤلفون: M, Plásilová, A, Gerinec, V, Ferák

المصدر: Ceska a slovenska oftalmologie : casopis Ceske oftalmologicke spolecnosti a Slovenske oftalmologicke spolecnosti. 54(5)

مصطلحات موضوعية: Slovakia, Roma, Cytochrome P-450 Enzyme System, Cytochrome P-450 CYP1B1, Humans, Point Mutation, Glaucoma, Aryl Hydrocarbon Hydroxylases, Prognosis, Polymerase Chain Reaction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::4cf386f9a38ac61d78628fc04a6e8e78
https://pubmed.ncbi.nlm.nih.gov/9818478

المؤلفون: L, Kádasi, H, Poláková, E, Feráková, T, Krivusová, S, Hudecová, I, Szomolayová, J, Strnová, I, Hruskovic, V, Ferák

المصدر: Bratislavske lekarske listy. 95(4)

مصطلحات موضوعية: Haplotypes, Phenylketonurias, Mutation, Humans, Phenylalanine Hydroxylase, DNA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::0ec8acbafc610e9dc6a5803b586de847
https://pubmed.ncbi.nlm.nih.gov/7812811

المؤلفون: E, Feráková, V, Ferák, L, Kádasi, H, Poláková, L, Hejcmanová, A, Pijacková

المصدر: Functional and developmental morphology. 2(2)

مصطلحات موضوعية: Czechoslovakia, Male, Roma, Haplotypes, Phenylketonurias, Chromosome Mapping, Humans, Phenylalanine Hydroxylase, Female, Polymorphism, Restriction Fragment Length

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::20dd7b9bf985ff45a9b0b53170b6a92f
https://pubmed.ncbi.nlm.nih.gov/1360274

المؤلفون: M. F. Pospíšil, V. Ferák

المصدر: Trends in Dermatoglyphic Research ISBN: 9789401074629

مصطلحات موضوعية: History, Anthropometric data, Anthropology, Ridge count, Dermatoglyphics, Connection (mathematics)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::dc91664ad34da1391ef1f22f8b195bda
https://doi.org/10.1007/978-94-009-2137-5_20

المؤلفون: A. Genčík, A. Genčíkova, V. Ferák

المصدر: Human Genetics. 61:193-197

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, Roma, genetic structures, Population, Population genetics, Disease, Biology, Gene Frequency, Ethnicity, Genetics, medicine, Humans, education, Allele frequency, Genetics (clinical), education.field_of_study, Incidence (epidemiology), Age Factors, Primary congenital glaucoma, Glaucoma, eye diseases, Human genetics, Czechoslovakia, Genetics, Population, Age of onset

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b3977e16ddc945457b42059fefe5e1e
https://doi.org/10.1007/bf00296440

المؤلفون: A. Mayerová, J. Gáliková, M. Vilímová, V. Ferák

المصدر: Human Heredity. 19:480-485

مصطلحات موضوعية: Male, Genetics, Haptoglobins, biology, Haptoglobin, Ethnic group, White People, Czechoslovakia, Genetics, Population, Gene Frequency, Ethnicity, biology.protein, Humans, Female, Allele frequency, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9dc753cdc811bb837c42ea8dcb72f6d
https://doi.org/10.1159/000152256

المؤلفون: V. Ferák, A. Genčík, A. Genčíkova

المصدر: Human Genetics. 61:198-200

مصطلحات موضوعية: Genetics, education.field_of_study, Roma, Incidence (epidemiology), Population, Selection coefficient, Glaucoma, Disease, Biology, Czechoslovakia, Consanguinity, Genetics, Population, Genetic drift, Ethnicity, Kinship, Humans, education, Inbreeding, Genetics (clinical), Founder effect

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1f3e2a37f8a85c32884d1dde82622f
https://doi.org/10.1007/bf00296441

المؤلفون: J, Karelová, M, Germániová, M, Hrubisko, V, Ferák

المصدر: Bratislavske lekarske listy. 77(2)

مصطلحات موضوعية: Adult, Male, Aging, Child, Preschool, Infant, Newborn, Humans, Infant, Female, Saliva, ABO Blood-Group System

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::4142b4971d2becdc1b4c66a978a899f0
https://pubmed.ncbi.nlm.nih.gov/7066714

المؤلفون: V, Ferák, Z, Kroupová, V, Mayer

المصدر: Bratislavske lekarske listy. 76(1)

مصطلحات موضوعية: Czechoslovakia, Consanguinity, Humans, Creutzfeldt-Jakob Syndrome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::59f6358cbbb7b6b13f67332d0ac9e20b
https://pubmed.ncbi.nlm.nih.gov/7020883

المؤلفون: V, Ferák, D, Chorvatovicová, J, Benko

المصدر: Bratislavske lekarske listy. 83(6)

مصطلحات موضوعية: Male, Child, Preschool, Infant, Newborn, Humans, Infant, Female, Seizures, Febrile

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::979f03633b1bfdf43a4070f892c333e7
https://pubmed.ncbi.nlm.nih.gov/4016552

المؤلفون: L, Kádasi, V, Ferák, M, Thurzová, M, Kvasnicová

المصدر: Bratislavske lekarske listy. 89(11)

مصطلحات موضوعية: Polymorphism, Genetic, X Chromosome, Genetic Carrier Screening, Humans, DNA Probes, Muscular Dystrophies, Polymorphism, Restriction Fragment Length, Pedigree

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::5e9bd29aaa74c53f692539b80fe984f6
https://pubmed.ncbi.nlm.nih.gov/2904832

المؤلفون: L, Kádasi, V, Ferák, A, Gencík, S, Demjén

المصدر: Bratislavske lekarske listy. 69(3)

مصطلحات موضوعية: Chromosome Aberrations, Cleft Palate, Male, Pregnancy, Cleft Lip, Infant, Newborn, Humans, Female, Genetic Counseling

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::cb879381920d3ec966a6996e9985954c
https://pubmed.ncbi.nlm.nih.gov/630441

المؤلفون: V, Ferák, L, Kádasi, M, Hrubisko, D, Siváková, E, Véghová

المصدر: Ceskoslovenska neurologie a neurochirurgie. 52(3)

مصطلحات موضوعية: Muscular Atrophy, Spinal, Charcot-Marie-Tooth Disease, Chromosomes, Human, Pair 1, Genetic Linkage, Antithrombin III, Humans, Duffy Blood-Group System, Isoamylase, Genes, Dominant, Pedigree

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::722f3888409a01364e97e1ac63bb43df
https://pubmed.ncbi.nlm.nih.gov/2582521

المؤلفون: J, Karelová, M, Germániová, M, Hrubisko, V, Ferák

المصدر: Bratislavske lekarske listy. 77(3)

مصطلحات موضوعية: Adult, Czechoslovakia, Humans, Child, ABO Blood-Group System

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::bf992a69f1ffadc7f58b809ee3102666
https://pubmed.ncbi.nlm.nih.gov/7074372

المؤلفون: A, Gencík, A, Gencíková, V, Ferák

المصدر: Bratislavske lekarske listy. 73(3)

مصطلحات موضوعية: Czechoslovakia, Consanguinity, Roma, Infant, Newborn, Humans, Glaucoma

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::087b43e37ebc3117879f27a8ae700076
https://pubmed.ncbi.nlm.nih.gov/7363126

المؤلفون: R, Brdicka, O, Stark, J, Srám, V, Ferák, A, Horínek, E, Zdárský

المصدر: Casopis lekaru ceskych. 127(4)

مصطلحات موضوعية: Genetic Markers, Genetic Carrier Screening, Genetic Diseases, Inborn, Humans, DNA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::1709ae5c2df0acbb3cf676b170d13f60
https://pubmed.ncbi.nlm.nih.gov/3162406