Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1755-8166

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search ; volume:14 ; number:1 ; day:24 ; month:7 ; year:2021 ; pages:1-9 ; date:12.2021
Molecular cytogenetics ; 14, Heft 1 (24.7.2021), 1-9, 12.2021

Creator: Vrachnis, Nikolaos
Papoulidis, Ioannis
Vrachnis, Dionysios
Siomou, Elisavet
Antonakopoulos, Nikolaos
Oikonomou, Stavroula
Zygouris, Dimitrios
Loukas, Nikolaos
Iliodromiti, Zoi
Pavlidou, Efterpi
Thomaidis, Loretta
Manolakos, Emmanouil

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13039-021-00557-y

URN: urn:nbn:de:101:1-2021102403551660807711

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

Last update: 15.08.2025, 7:29 AM CEST

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Associated

Vrachnis, Nikolaos
Papoulidis, Ioannis
Vrachnis, Dionysios
Siomou, Elisavet
Antonakopoulos, Nikolaos
Oikonomou, Stavroula
Zygouris, Dimitrios
Loukas, Nikolaos
Iliodromiti, Zoi
Pavlidou, Efterpi
Thomaidis, Loretta
Manolakos, Emmanouil
SpringerLink (Online service)

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Partial deletion of chromosome 6p causing developmental delay and mild dysmorphisms in a child: molecular and developmental investigation and literature search

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Other Objects (12)

Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Staged developmental mapping and X chromosome transcriptional dynamics during mouse spermatogenesis

Genetic analysis of BRPF1 exon deletion variant causing intellectual developmental disorder with dysmorphic facies and ptosis in a Chinese family

Developmental and clinical pragmatics

Homology and developmental genes

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

Chromosome 12q24.31-q24.33 deletion causes multiple dysmorphic features and developmental delay: First mosaic patient and overview of the phenotype related to 12q24qter defects

Developmental trajectories of executive functions in 22q11.2 deletion syndrome

Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation

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Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

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Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Staged developmental mapping and X chromosome transcriptional dynamics during mouse spermatogenesis

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Developmental and clinical pragmatics

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Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation

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Neuro-developmental syndrome at the border between CANPMR syndrome and chromosome 1p32-p31 deletion syndrome

A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms

Social cognition in 22q11.2 deletion syndrome and idiopathic developmental neuropsychiatric disorders

Staged developmental mapping and X chromosome transcriptional dynamics during mouse spermatogenesis

Genetic analysis of BRPF1 exon deletion variant causing intellectual developmental disorder with dysmorphic facies and ptosis in a Chinese family

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