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1دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
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2
المؤلفون: P D, Cotter, S, Kaffe, L, Li, I F, Gershin, K, Hirschhorn
المصدر: American journal of medical genetics. 102(1)
مصطلحات موضوعية: Chromosome Aberrations, Family Health, Male, Genotype, Chromosome Mapping, DNA, Telomere, Chromosome Banding, Pedigree, Child, Preschool, Gene Duplication, Karyotyping, Chromosome Inversion, Humans, Female, Chromosome Deletion, Chromosomes, Human, Pair 4, In Situ Hybridization, Fluorescence, Microsatellite Repeats
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3
المؤلفون: P D, Cotter, S, Kaffe, L D, McCurdy, M, Jhaveri, J P, Willner, K, Hirschhorn
المصدر: American journal of medical genetics. 70(1)
مصطلحات موضوعية: Adult, Chromosomes, Human, Pair 14, Genetic Markers, Male, Polymorphism, Genetic, Chromosome Mapping, Infant, Aneuploidy, Translocation, Genetic, Pedigree, Genomic Imprinting, Prenatal Diagnosis, Humans, Abnormalities, Multiple, Female, Lymphocytes
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4
المؤلفون: Ben Zion Garty, R. Dagan, Bella Eisenstein, N. Gadoth, Judith Sandbank, S. Kaffe
مصطلحات موضوعية: Male, medicine.medical_specialty, Pathology, Microcephaly, Nephrotic Syndrome, Genes, Recessive, Nuclear Family, Consanguinity, Internal medicine, Cerebellum, Intellectual Disability, Muscle Hypertonia, Genetics, medicine, Humans, Abnormalities, Multiple, Congenital nephrotic syndrome, Genetics (clinical), Growth Disorders, Sclerosis, Psychomotor retardation, business.industry, Infant, Glomerulonephritis, Syndrome, medicine.disease, Galloway Mowat syndrome, Glomerular Mesangium, Pedigree, Endocrinology, Mesangium, Mesangial proliferative glomerulonephritis, Female, medicine.symptom, business, Nephrotic syndrome, Head, Research Article
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69cb8822e40a353268d2945e631e3af4
https://europepmc.org/articles/PMC1049672/ -
5دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
6
المؤلفون: K. Hirschhorn, S. Kaffe
المصدر: Prenatal Diagnosis. 12:976-976
مصطلحات موضوعية: Obstetrics and Gynecology, Genetics (clinical)
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7
المؤلفون: I Nissenkorn, S. Kaffe, I. Ben-Sira, Yuval Yassur, R.M. Goodman
المصدر: American Journal of Ophthalmology. 94:338-343
مصطلحات موضوعية: Adult, Male, Retinal degeneration, Peripheral retinoschisis, Retinoschisis, Chromosome Disorders, Macular pigmentary changes, Biology, Retinal Diseases, medicine, Humans, Child, Aged, Genes, Dominant, Chromosome Aberrations, Genetics, Genetic heterogeneity, Retinal Degeneration, Infant, Middle Aged, Peripheral Retinal Degeneration, medicine.disease, Pedigree, Ophthalmology, Child, Preschool, Female, Three generations
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d759f6aa4ad0505494e063fb6263608
https://doi.org/10.1016/0002-9394(82)90359-2 -
8
المؤلفون: M Sippola, D J Prockop, S Kaffe
المصدر: Journal of Biological Chemistry. 259:14094-14100
مصطلحات موضوعية: chemistry.chemical_classification, Circular dichroism, medicine.diagnostic_test, Proteolysis, Procollagen N-Endopeptidase, Cell Biology, Biochemistry, Amino acid, chemistry.chemical_compound, Procollagen peptidase, chemistry, medicine, Cyanogen bromide, Sodium dodecyl sulfate, Molecular Biology, Polyacrylamide gel electrophoresis
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::61e354b23580c541abe87cb9c865fcdc
https://doi.org/10.1016/s0021-9258(18)89861-1 -
9
المؤلفون: Charles B. Brill, Lillian Y. F. Hsu, H J Kim, S Kaffe, Kurt Hirschhorn
المصدر: Journal of Medical Genetics. 14:447-451
مصطلحات موضوعية: Male, Mosaicism, G banding, Ring chromosome, Infant, Chromosome, Karyotype, Anatomy, Biology, Staining, Cleft Palate, Child, Preschool, Intellectual Disability, Karyotyping, Genetics, Humans, Constitutive heterochromatin, Supernumerary, Child, Small supernumerary marker chromosome, Genetics (clinical), Research Article
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6287d274f259ec56b6b13bf11bb2627c
https://doi.org/10.1136/jmg.14.6.447 -
10دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل.