Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Aniridia, balanced chromosomal rearrangements"'
Autor:
Tatyana A. Vasilyeva, Andrey V. Marakhonov, Marina E. Minzhenkova, Zhanna G. Markova, Nika V. Petrova, Natella V. Sukhanova, Philipp A. Koshkin, Denis V. Pyankov, Ilya V. Kanivets, Sergey A. Korostelev, Irina A. Krynskaya, Nadezhda V. Shilova, Sergey I. Kutsev, Vitaly V. Kadyshev, Rena A. Zinchenko
Publikováno v:
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-5 (2020)
Abstract Background Because of the significant occurrence of “WAGR-region” deletions among de novo mutations detected in congenital aniridia, DNA diagnosis is critical for all sporadic cases of aniridia due to its help in making an early diagnosi
Externí odkaz:
https://doaj.org/article/5a4f4c93fb51459caf26f894f64b28c5
Autor:
Zhanna G. Markova, Marina E. Minzhenkova, Natella V. Sukhanova, Nadezhda V. Shilova, Nika V. Petrova, Tatyana A. Vasilyeva, Denis V Pyankov, Rena A. Zinchenko, V. V. Kadyshev, Ilya V. Kanivets, Irina A. Krynskaya, Sergey Korostelev, Andrey V. Marakhonov, Sergey I. Kutsev, Philipp Aleksandrovich Koshkin
Publikováno v:
BMC Medical Genomics, Vol 13, Iss S8, Pp 1-5 (2020)
BMC Medical Genomics
BMC Medical Genomics
Background Because of the significant occurrence of “WAGR-region” deletions among de novo mutations detected in congenital aniridia, DNA diagnosis is critical for all sporadic cases of aniridia due to its help in making an early diagnosis of WAGR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e207212ba6cf5f8b6e5af4ac19022a4
https://doi.org/10.1186/s12920-020-00790-1
https://doi.org/10.1186/s12920-020-00790-1
Akademický článek
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