Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Dilihan Gumus"'
Autor:
Reinhard Ullmann, Nuran Sabir, Dilihan Gumus, Mine Cinbiş, Anne Steininger, Baki Yagci, Osvaldo M. Mutchinick, Emre Tepeli, C. Nur Semerci, Muhterem Bahçe, Serap Özden, Jazmín Arteaga
Publikováno v:
American Journal of Medical Genetics Part A. :1724-1729
We report on a patient with partial monosomy 6p and partial trisomy 12q identified by fluorescent in situ hybridization (FISH) and array-based comparative genomic hybridization (aCGH). She had a complex phenotype characterized by mental retardation (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2229de342c59a21c30d865462798b798
https://doi.org/10.1002/ajmg.a.33383
https://doi.org/10.1002/ajmg.a.33383
Autor:
Nadine Norton, Fikret Erdogan, Reinhard Ullmann, Lyudmila Georgieva, Wei Chen, Murat Sari, Hans-Hilger Ropers, Michael Conlon O'Donovan, George Kirov, Dilihan Gumus, Michael John Owen
Publikováno v:
Human Molecular Genetics
Copy number variations (CNVs) account for a substantial proportion of human genomic variation, and have been shown to cause neurodevelopmental disorders. We sought to determine the relevance of CNVs to the aetiology of schizophrenia (SZ). Whole-genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::522e8da6c9ee6e6f6d10044ffd783409
https://pubmed.ncbi.nlm.nih.gov/17989066
https://pubmed.ncbi.nlm.nih.gov/17989066