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Article

Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families.

American journal of medical genetics. Part A - 1 Jan 2012

Zilina O, Reimand T, Zjablovskaja P, Männik K, Männamaa M, Traat A, Puusepp-Benazzouz H, Kurg A, Ounap K

Abstract excerpt

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Share to Child, Preschool
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 22105961
DOI: 10.1002/ajmg.a.34378

Genes

FOXP2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families.PMID 22105961Read ↗

7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder.Semantic proximity Read ↗

[Clinical phenotype of a patient with FOXP1 deletion].Semantic proximity Read ↗

Deciphering the genetic basis of speech and language disorders.Semantic proximity Read ↗

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Case Report of Suspected Gonadal Mosaicism in FOXP1-Related Neurodevelopmental Disorder.Semantic proximity Read ↗

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population.Semantic proximity Read ↗

Prospective investigation of FOXP1 syndrome.Semantic proximity Read ↗

Identification of a novel nonsense mutation in the FOXP3 gene in a fetus with hydrops—Expanding the phenotype of IPEX syndromeSemantic proximity Read ↗

3p14.1 de novo microdeletion involving the FOXP1 gene in an adult patient with autism, severe speech delay and deficit of motor coordination.Semantic proximity Read ↗

Novel FOXP2 Variant Associated with Speech and Language Dysfunction in a Chinese Family and literature reviewSemantic proximity Read ↗

Phenotype of FOXP2 haploinsufficiency in a mother and son.Semantic proximity Read ↗

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?Semantic proximity Read ↗

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