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1كتاب
المؤلفون: Saygili S., Caliskan S., Ozaltin F.
مصطلحات موضوعية: adenine, arginine, glutamic acid, guanine, lysine, methionine, thymine, homeodomain protein, HOXA11 protein, human, transcription factor, chronic kidney failure, congenital anomalies of the kidney and urinary tract, consanguineous marriage, cryptorchism, gene, genetic counseling, genetic variability, growth retardation, heterozygosity, homozygosity, HOXA11 gene, hypothyroidism, kidney malformation, Letter, molecular pathology, nonhuman, phenotype, polyneuropathy, Sanger sequencing
العلاقة: Pediatric Nephrology; Diğer; https://doi.org/10.1007/s00467-022-05756-2Test; https://hdl.handle.net/20.500.12831/19459Test; 38; 933; 934; 2-s2.0-85140004110
الإتاحة: https://doi.org/10.1007/s00467-022-05756-2Test
https://doi.org/20.500.12831/19459Test
https://hdl.handle.net/20.500.12831/19459Test -
2كتاب
المساهمون: Ahmad, SI, Cavanna, A, Termine, C
مصطلحات موضوعية: article, attention deficit disorder, behavior therapy, clinical assessment, clinical feature, depression, diagnostic and statistical manual of mental disorder, diagnostic value, gene expression regulation, genetic susceptibility, genetic variability, Gilles de la Tourette syndrome, human, international classification of disease, mini mental state examination, molecular pathology, obsessive compulsive disorder, personality disorder, priority journal, psychopharmacotherapy, relaxation training, self monitoring, tic, unspecified side effect, differential diagnosi, review
العلاقة: info:eu-repo/semantics/altIdentifier/isbn/978-1-4614-0652-5; info:eu-repo/semantics/altIdentifier/pmid/22411257; info:eu-repo/semantics/altIdentifier/wos/WOS:000333978900030; ispartofbook:Neurodegenerative Diseases; volume:724; firstpage:375; lastpage:383; numberofpages:9; serie:ADVANCES IN EXPERIMENTAL MEDICINE AND BIOLOGY; alleditors:Ahmad, SI; https://hdl.handle.net/10281/410979Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84859512403
