Výsledky vyhledávání - "Consecutive deletions"

Akademický článek

First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient

Autor: Maysoon Alsagob, Mustafa A. Salih, Muddathir H. A. Hamad, Yusra Al-Yafee, Jawaher Al-Zahrani, Albandary Al-Bakheet, Michael Nester, Nadia Sakati, Salma M. Wakil, Ali AlOdaib, Dilek Colak, Namik Kaya

Publikováno v: Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-6 (2019)

Abstract 15q13.3 syndrome is associated with a wide spectrum of neurological disorders. Among a cohort of 150 neurodevelopmental cases, we identified two patients with two close proximity interstitial hemizygous deletions on chromosome 15q13. Using h

Externí odkaz: https://doaj.org/article/74f03fe71e934a9d8b9467422ded30d0

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First report of two successive deletions on chromosome 15q13 cytogenetic bands in a boy and girl: additional data to 15q13.3 syndrome with a report of high IQ patient

Autor: Yusra Alyafee, Salma M. Wakil, N. Kaya, Michael Nester, Muddathir H. Hamad, Dilek Colak, Maysoon Alsagob, Ali Al-Odaib, Nadia Sakati, Mustafa A. Salih, Jawaher Al-Zahrani, Albandary Al-Bakheet

Publikováno v: Molecular Cytogenetics, Vol 12, Iss 1, Pp 1-6 (2019)
Molecular Cytogenetics

15q13.3 syndrome is associated with a wide spectrum of neurological disorders. Among a cohort of 150 neurodevelopmental cases, we identified two patients with two close proximity interstitial hemizygous deletions on chromosome 15q13. Using high-densi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::485113d22fe6a730ad5d4369adee9e85
https://doi.org/10.1186/s13039-019-0432-6

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Akademický článek

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