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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

Crossref DOI link: https://doi.org/10.1186/s13039-019-0432-6

Published Online: 2019-05-18

Published Print: 2019-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Alsagob, Maysoon

Salih, Mustafa A.

Hamad, Muddathir H. A.

Al-Yafee, Yusra

Al-Zahrani, Jawaher

Al-Bakheet, Albandary

Nester, Michael

Sakati, Nadia

Wakil, Salma M.

AlOdaib, Ali

Colak, Dilek

Kaya, Namik https://orcid.org/0000-0001-8912-7507
Funding

Funding for this research was provided by:

King Salman Center for Disability Research (02-R-0029-NE-02-AU-1, 2180 004)

King Abdulaziz City for Science and Technology (14-MED2007-20, 11-BIO2072-20)

Deanship of Scientific Research, King Saud University (RGP-VPP- 301)
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Text and Data Mining valid from 2019-05-18

Version of Record valid from 2019-05-18
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Article History

Received: 13 February 2019

Accepted: 1 May 2019

First Online: 18 May 2019

Authors’ information

: Michael Nester - recently retired from KFSHR.

: The patients were ascertained under one of the King Faisal Specialist Hospital and Research Center’s institutionally approved IRB protocols (KFSHRC’s Research Advisory Council Committees (RAC# 2120022 2040042, 2030046, 2040024). Before the sample collection, the patients and/or parents (legal guardians) signed the written informed consents.

: Written informed consents were obtained from the related parties.

: The authors declare that they have no competing interests.

: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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