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المؤلفون: S E Pound, Peter C. Harris, M L Watson, Anna Maria Frischauf, S. Thomas, P M Pignatelli, A F Wright, A. Snarey, A M Macnicol
المصدر: Journal of Medical Genetics. 32:208-212
مصطلحات موضوعية: Adult, Genetic Markers, Male, TRPP Cation Channels, Genetic Linkage, Autosomal dominant polycystic kidney disease, Locus (genetics), Biology, urologic and male genital diseases, Genetic linkage, Genetics, medicine, Humans, Gene, Genetics (clinical), Aged, PKD1, urogenital system, Haplotype, Proteins, Middle Aged, Polycystic Kidney, Autosomal Dominant, medicine.disease, female genital diseases and pregnancy complications, Haplotypes, Genetic marker, Mutation, New mutation, Female, Chromosomes, Human, Pair 16, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29c69932fb28fa4b8b5e665f02d6bd84Test
https://doi.org/10.1136/jmg.32.3.208Test -
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المؤلفون: J F Clayton
المصدر: Journal of Medical Genetics. 23:35-39
مصطلحات موضوعية: Male, Risk, Genetics, X Chromosome, Models, Genetic, Disease, Biology, Pedigree, Recurrence risk, Sex Chromosome Aberrations, New mutation, Genotype, Humans, Female, Genetic risk, Software, Genetics (clinical), X chromosome, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c0f769fbf9f5526a29f10a8aeaf66bfTest
https://doi.org/10.1136/jmg.23.1.35Test -
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المصدر: Journal of medical genetics. 11(2)
مصطلحات موضوعية: Marfan syndrome, musculoskeletal diseases, Adult, Male, Pediatrics, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Marfan Syndrome, Fingers, Gene Frequency, Genetics, Medicine, Humans, Syndactyly, Israel, Genetics (clinical), Genes, Dominant, S syndrome, business.industry, Infant, Newborn, Articles, Toes, medicine.disease, Penetrance, Infant newborn, Pedigree, body regions, Phenotype, Polysyndactyly, Jews, New mutation, Egypt, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::538f2b41f62e3f4e7283370b4af9a2e4Test
https://pubmed.ncbi.nlm.nih.gov/4366482Test