المؤلفون: T.W.A. de Bruin, Bradley E. Aouizerat, Hooman Allayee, Aldons J. Lusis, Geesje M. Dallinga-Thie, J.L. Rotter, Rita M. Cantor, R.M. Krauss, C.D. Lanning

المساهمون: Other departments, Interne Geneeskunde, RS: NUTRIM School of Nutrition and Translational Research in Metabolism

المصدر: American journal of human genetics, 63(2), 577-585. Cell Press
American Journal of Human Genetics, 63(2), 577-585. Cell Press

مصطلحات موضوعية: Male, Genetic-linkage analysis, Apolipoprotein B, Genetic Linkage, Hyperlipidemia, Familial Combined, Coronary Disease, 030204 cardiovascular system & hematology, Phosphatidylcholine-Sterol O-Acyltransferase, 0302 clinical medicine, Hyperlipidemia, Genetics(clinical), Genetics (clinical), Netherlands, Genetics, 0303 health sciences, education.field_of_study, biology, Chromosome Mapping, Middle Aged, 3. Good health, Lipoproteins, LDL, Phenotype, Chromosomes, Human, Pair 6, Female, lipids (amino acids, peptides, and proteins), Research Article, Adult, Atherogenic lipoprotein phenotype, Familial combined hyperlipidemia, Population, Locus (genetics), White People, 03 medical and health sciences, Genetic linkage, Cholesterylester transfer protein, medicine, Humans, Family, Complex disease, Apolipoproteins C, education, Apolipoproteins A, Glycoproteins, 030304 developmental biology, Apolipoprotein A-I, Superoxide Dismutase, Chromosomes, Human, Pair 11, medicine.disease, Cholesterol Ester Transfer Proteins, Receptors, LDL, LDL receptor, biology.protein, Apolipoprotein C-II, Carrier Proteins, Chromosomes, Human, Pair 19, Chromosomes, Human, Pair 16, Lipoprotein

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebd307a24da4be75548a987551a70f6eTest
https://doi.org/10.1086/301983Test

المؤلفون: Casari G., De Fusco M., Ciarmatori S., Zeviani M., Mora M., Fernandez P., De Michele G., Filla A., Cocozza S., Marconi R., Durr A., Fontaine B., Ballabio A.

المساهمون: Casari, G., De Fusco, M., Ciarmatori, S., Zeviani, M., Mora, M., Fernandez, P., De Michele, G., Filla, A., Cocozza, S., Marconi, R., Durr, A., Fontaine, B., Ballabio, A.

مصطلحات موضوعية: ATPases Associated with Diverse Cellular Activitie, Adult, Amino Acid Sequence, Cell Nucleu, Chromosomes, Human, Pair 16, Cloning, Molecular, DNA, Complementary, Female, Fetu, Frameshift Mutation, Italy, Male, Metalloendopeptidase, Mitochondria, Molecular Sequence Data, Muscle, Skeletal, Oxidative Phosphorylation, Pedigree, RNA, Messenger, Sequence Analysis, Sequence Homology, Amino Acid, Spastic Paraplegia, Hereditary

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/9635427; info:eu-repo/semantics/altIdentifier/wos/WOS:000074205700009; volume:93; issue:6; firstpage:973; lastpage:983; numberofpages:11; journal:CELL; http://hdl.handle.net/11577/3354503Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0032511186

الإتاحة: https://doi.org/10.1016/S0092-8674Test(00)81203-9
http://hdl.handle.net/11577/3354503Test

المؤلفون: Sampson, J., Maheshwar, M., Aspinwall, R., Thompson, P., Cheadle, J., Ravine, D., Roy, S., Haan, E., Bernstein, J., Harris, P.

المصدر: http://dx.doi.org/10.1086/514888Test.

مصطلحات موضوعية: Chromosomes, Human, Pair 16, Humans, Polycystic Kidney Diseases, Polycystic Kidney, Autosomal Dominant, Tuberous Sclerosis, Proteins, Tumor Suppressor Proteins, Repressor Proteins, Electrophoresis, Gel, Pulsed-Field, In Situ Hybridization, Fluorescence, Chromosome Mapping, Restriction Mapping, Karyotyping, Nuclear Family, Gene Rearrangement, Sequence Deletion, Mutation, Mosaicism, Genes, Tumor Suppressor, Introns, Adolescent, Adult, Child

العلاقة: American Journal of Human Genetics, 1997; 61(4):843-851; http://hdl.handle.net/2440/6919Test; Haan, E. [0000-0002-7310-5124]

الإتاحة: https://doi.org/10.1086/514888Test
http://hdl.handle.net/2440/6919Test

المؤلفون: Yu, S., Mangelsdorf, M., Hewett, D., Hobson, L., Baker, E., Eyre, H., Lapsys, N., Le Paslier, D., Doggett, N., Sutherland, G., Richards, R.

مصطلحات موضوعية: Chromosomes, Human, Pair 16, Humans, Chromosome Fragility, DNA, Satellite, Blotting, Southern, Cloning, Molecular, Polymerase Chain Reaction, Gene Amplification, Base Composition, Base Sequence, Minisatellite Repeats, Polymorphism, Genetic, Chromosome Fragile Sites, Molecular Sequence Data

العلاقة: Cell, 1997; 88(3):367-374; http://hdl.handle.net/2440/7103Test

الإتاحة: https://doi.org/10.1016/S0092-8674Test(00)81875-9
http://hdl.handle.net/2440/7103Test