Genetic determinants of global developmental delay and intellectual disability in Ukrainian children

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Genetic determinants of global developmental delay and intellectual disability in Ukrainian children ; volume:16 ; number:1 ; day:27 ; month:3 ; year:2024 ; pages:1-10 ; date:12.2024
Journal of neurodevelopmental disorders ; 16, Heft 1 (27.3.2024), 1-10, 12.2024

Creator: Shchubelka, Khrystyna
Turova, Liudmyla
Wolfsberger, Walter
Kalanquin, Kelly
Williston, Krista
Kurutsa, Oleksii
Makovetska, Anastasiia
Hasynets, Yaroslava
Mirutenko, Violeta
Vakerych, Mykhailo
Oleksyk, Taras K.

Contributor: SpringerLink (Online service)

DOI: 10.1186/s11689-024-09528-x

URN: urn:nbn:de:101:1-2406130853476.901491198497

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

Last update: 14.08.2025, 10:49 AM CEST

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Associated

Shchubelka, Khrystyna
Turova, Liudmyla
Wolfsberger, Walter
Kalanquin, Kelly
Williston, Krista
Kurutsa, Oleksii
Makovetska, Anastasiia
Hasynets, Yaroslava
Mirutenko, Violeta
Vakerych, Mykhailo
Oleksyk, Taras K.
SpringerLink (Online service)

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Genetic determinants of global developmental delay and intellectual disability in Ukrainian children

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Other Objects (12)

Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions

Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability

Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly

A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy

Genetic analysis of 280 children with unexplained developmental delay or intellectual disability using whole exome sequencing

Inherited unbalanced translocation (4p16.3p15.32 duplication/8p23.3p23.2deletion) in the four generation pedigree with intellectual disability/developmental delay

Developmental associations between cognition and adaptive behavior in intellectual and developmental disability

Meeting emotional needs in intellectual disability : the developmental approach

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

Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions

Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability

Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly

A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy

Genetic analysis of 280 children with unexplained developmental delay or intellectual disability using whole exome sequencing

Inherited unbalanced translocation (4p16.3p15.32 duplication/8p23.3p23.2deletion) in the four generation pedigree with intellectual disability/developmental delay

Developmental associations between cognition and adaptive behavior in intellectual and developmental disability

Meeting emotional needs in intellectual disability : the developmental approach

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

Subtelomeric FISH analysis in 76 patients with syndromic developmental delay/intellectual disability

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions

Microduplication in the 2p16.1p15 chromosomal region linked to developmental delay and intellectual disability

CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

Copy number variation analysis in 189 Romanian patients with global developmental delay/intellectual disability

Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly

A novel NAA10 variant with impaired acetyltransferase activity causes developmental delay, intellectual disability, and hypertrophic cardiomyopathy

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Inherited unbalanced translocation (4p16.3p15.32 duplication/8p23.3p23.2deletion) in the four generation pedigree with intellectual disability/developmental delay

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Meeting emotional needs in intellectual disability : the developmental approach

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

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