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المؤلفون: M. H. Breuning, A. van Haeringen
المصدر: Compendium kindergeneeskunde ISBN: 9789036817912
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::1f6ac990fa910c8253541449471b1dcf
https://doi.org/10.1007/978-90-368-1792-9_47 -
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المؤلفون: N A, Doggett, M H, Breuning, D F, Callen
المصدر: Cytogenetic and Genome Research. 72:271-293
مصطلحات موضوعية: Genetic Markers, Genetic Linkage, Gene Expression, Hybrid Cells, Biology, Mice, Chromosome 16, Species Specificity, Genetic linkage, Neoplasms, Genetics, Animals, Humans, Cloning, Molecular, Chromosomes, Artificial, Yeast, Molecular Biology, Genetics (clinical), Genetic Diseases, Inborn, Chromosome Mapping, Cosmids, Rats, Genetic marker, Cosmid, Cattle, Chromosomes, Human, Pair 16
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المؤلفون: Y, Hilhorst-Hofstee, A J H A, Scholte, M E B, Rijlaarsdam, A, van Haeringen, L J, Kroft, M, Reijnierse, C A L, Ruivenkamp, M I M, Versteegh, G, Pals, M H, Breuning
المصدر: Clinical genetics. 83(4)
مصطلحات موضوعية: Adult, Male, Chromosomes, Human, Pair 15, Adolescent, Aortic Aneurysm, Thoracic, DNA Copy Number Variations, Middle Aged, Pedigree, Child, Preschool, Humans, Female, Genetic Predisposition to Disease, Smad3 Protein, Chromosome Deletion, Child, Aged
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المصدر: Nederlands tijdschrift voor geneeskunde. 149(9)
مصطلحات موضوعية: Humans, Receptors, Cell Surface, Kidney, Ultrasonography, Prenatal, Polycystic Kidney, Autosomal Recessive
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::3a6056046c76a1f2d532bb460a4db80f
https://pubmed.ncbi.nlm.nih.gov/15771341 -
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المؤلفون: P E M, Taschner, M, Losekoot, M H, Breuning, I, Hofman, O P, van Diggelen
المصدر: Nederlands tijdschrift voor geneeskunde. 149(6)
مصطلحات موضوعية: Membrane Glycoproteins, Tripeptidyl-Peptidase 1, DNA Mutational Analysis, Membrane Proteins, Aminopeptidases, Genetic Heterogeneity, Neuronal Ceroid-Lipofuscinoses, Endopeptidases, Humans, Genetic Testing, Thiolester Hydrolases, Serine Proteases, Child, Dipeptidyl-Peptidases and Tripeptidyl-Peptidases, Molecular Chaperones, Peptide Hydrolases
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::29ec3909347d120205fa817d9b2a4fdc
https://pubmed.ncbi.nlm.nih.gov/15730038 -
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المؤلفون: M, Losekoot, A J, Broekman, M H, Breuning, E J P, de Koning, J A, Romijn, J A, Maassen
المصدر: Nederlands tijdschrift voor geneeskunde. 149(3)
مصطلحات موضوعية: Adult, Male, Nuclear Proteins, Phosphoproteins, Pedigree, DNA-Binding Proteins, Diabetes Mellitus, Type 2, Hepatocyte Nuclear Factor 4, Glucokinase, Hepatocyte Nuclear Factor 1, Mutation, Humans, Female, Hepatocyte Nuclear Factor 1-alpha, Age of Onset, Transcription Factors
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::8fa4c8343a8914a3326acf6d8da5b028
https://pubmed.ncbi.nlm.nih.gov/15693590 -
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المؤلفون: Christi J, van Asperen, M A, Jonker, C E, Jacobi, J E M, van Diemen-Homan, E, Bakker, M H, Breuning, J C, van Houwelingen, G H, de Bock
المصدر: Cancer epidemiology, biomarkersprevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 13(1)
مصطلحات موضوعية: Male, Ovarian Neoplasms, Logistic Models, Genes, BRCA2, Genes, BRCA1, Humans, Breast Neoplasms, Family, Female, Risk Assessment
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::d0f2946119b91f3d5e730598623ac139
https://pubmed.ncbi.nlm.nih.gov/14744738 -
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المؤلفون: M H, Breuning, N A T C, Hamdy
المصدر: Nederlands tijdschrift voor geneeskunde. 147(6)
مصطلحات موضوعية: Kidney Calculi, Cystinuria, Membrane Glycoproteins, Genotype, Mutation, Prevalence, Amino Acid Transport Systems, Basic, Humans, Amino Acids, Carrier Proteins, Netherlands
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::52d76710503d86f80dafac0503ab4c05
https://pubmed.ncbi.nlm.nih.gov/12848061 -
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المؤلفون: M H, Breuning
المصدر: Nederlands tijdschrift voor geneeskunde. 146(43)
مصطلحات موضوعية: Phenotype, Velopharyngeal Insufficiency, Chromosomes, Human, Pair 22, Face, DiGeorge Syndrome, Schizophrenia, Humans, Abnormalities, Multiple, Female, Gene Deletion, Signal Transduction
URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::cc2c22eedb9fefcfd4492c1e7a850bfe
https://pubmed.ncbi.nlm.nih.gov/12428463