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1دورية أكاديمية
المؤلفون: P J Bridge, F P Bernier
المساهمون: The Pennsylvania State University CiteSeerX Archives
وصف الملف: application/pdf
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2
المؤلفون: K N, Alagramam, H, Yuan, M H, Kuehn, C L, Murcia, S, Wayne, C R, Srisailpathy, R B, Lowry, R, Knaus, L, Van Laer, F P, Bernier, S, Schwartz, C, Lee, C C, Morton, R F, Mullins, A, Ramesh, G, Van Camp, G S, Hageman, R P, Woychik, R J, Smith, G S, Hagemen
المصدر: Human molecular genetics
مصطلحات موضوعية: Adult, Male, animal structures, Genetic Linkage, Usher syndrome, Blotting, Western, DNA Mutational Analysis, Molecular Sequence Data, Nonsense mutation, Cadherin Related Proteins, Protocadherin, Deafness, Biology, Retina, Mice, Exon, Fetus, CDH23, otorhinolaryngologic diseases, Genetics, medicine, Animals, Humans, Amino Acid Sequence, Protein Precursors, Molecular Biology, In Situ Hybridization, Fluorescence, Polymorphism, Single-Stranded Conformational, Genetics (clinical), Sequence Homology, Amino Acid, medicine.diagnostic_test, Reverse Transcriptase Polymerase Chain Reaction, Gene Expression Profiling, Usher Syndrome Type 1, Syndrome, General Medicine, Blotting, Northern, Cadherins, medicine.disease, Molecular biology, Cochlea, Pedigree, Mutation, Female, PCDH15, Fluorescence in situ hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6524cf5f1965b23c42339cc0196a7945Test
https://hdl.handle.net/10067/358410151162165141Test -
3
المؤلفون: N J, Leonard, F P, Bernier, N, Rudd, G A, Machin, F, Bamforth, S, Bamforth, P, Grundy, C, Johnson
المصدر: American journal of medical genetics. 61(3)
مصطلحات موضوعية: Adult, Chromosome Aberrations, Male, Beckwith-Wiedemann Syndrome, Humans, Female, Chorion, DNA, Twins, Monozygotic
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::aec8006bbb1b0540c522c7aab2f0214dTest
https://pubmed.ncbi.nlm.nih.gov/8741870Test