The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2045-2322

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families ; volume:12 ; number:1 ; day:7 ; month:11 ; year:2022 ; pages:1-12 ; date:12.2022
Scientific reports ; 12, Heft 1 (7.11.2022), 1-12, 12.2022

Creator: Al-Kasbi, Ghalia
Al-Murshedi, Fathiya
Al-Kindi, Adila
Al-Hashimi, Nadia
Al-Thihli, Khalid
Al-Saegh, Abeer
Al-Futaisi, Amna
Al-Mamari, Watfa
Al-Asmi, Abdullah
Bruwer, Zandre
Al-Kharusi, Khalsa
Al-Rashdi, Samiya
Zadjali, Fahad
Al-Yahyaee, Said
Al-Maawali, Almundher

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-022-22036-z

URN: urn:nbn:de:101:1-2023012110565852067899

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:23 AM CEST

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Associated

Al-Kasbi, Ghalia
Al-Murshedi, Fathiya
Al-Kindi, Adila
Al-Hashimi, Nadia
Al-Thihli, Khalid
Al-Saegh, Abeer
Al-Futaisi, Amna
Al-Mamari, Watfa
Al-Asmi, Abdullah
Bruwer, Zandre
Al-Kharusi, Khalsa
Al-Rashdi, Samiya
Zadjali, Fahad
Al-Yahyaee, Said
Al-Maawali, Almundher
SpringerLink (Online service)

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The diagnostic yield, candidate genes, and pitfalls for a genetic study of intellectual disability in 118 middle eastern families

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Other Objects (12)

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Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability : the WASH complex member SWIP

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Genetics of autosomal recessive intellectual disability

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Targeted next generation sequencing in 112 Chinese patients with intellectual disability/developmental delay: novel mutations and candidate gene

Identification of a novel candidate gene for non-syndromic autosomal recessive intellectual disability : the WASH complex member SWIP

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Calcium channelopathies and intellectual disability: a systematic review

Single gene microdeletions and microduplication of 3p26.3 in three unrelated families: CNTN6 as a new candidate gene for intellectual disability

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