15q11.2 Microdeletion Latest Advances

Refining the electroclinical phenotype of 15q11.2 microdeletion: EEG biomarker overlap with Angelman syndrome.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: April 15, 2026

The Association of Environmental Variables with Intelligence and Well-Being in Copy Number Variation (CNV) Carriers.

Journal: Research square

Published: February 23, 2026

Prenatal diagnosis and pregnancy outcome of fetuses with 15q11.2 BP1-BP2 microdeletion syndrome: a single-center retrospective study of 34 cases.

Journal: BMC pediatrics

Published: February 18, 2026

Prenatal diagnosis of familial concomitant 2q11.1q11.2 deletion and 15q11.2 deletion in a pregnancy associated with no apparently phenotypic abnormality.

Journal: Taiwanese journal of obstetrics & gynecology

Published: January 02, 2026

Outcomes and Management of Pregnancies Screening Positive for Microdeletions 22q11.2, 15q11.2, 1p36, 4p, or 5p: A Retrospective Cohort Study.

Journal: The application of clinical genetics

Published: December 24, 2025

Genomics of Complex Neurodevelopmental Disorders with Variable Epilepsy Phenotypes: A Clinical Review of Dup15q Syndrome.

Journal: Genes

Published: December 20, 2025

Diagnostic value of karyotyping, CMA/CNV-seq, and WES in fetuses with thickened nuchal translucency: perinatal and two-year follow-up outcomes.

Journal: BMC medical genomics

Published: November 10, 2025

White matter microstructure differences between 15q11.2 copy number variation carriers and non-carriers in mid-to-late life.

Journal: Translational psychiatry

Published: September 25, 2025

Simultaneous Le Fort III and Le Fort I Osteotomies for Rare Midfacial Hypoplasia in a Patient with 15q11.2 Microdeletion-A Multidisciplinary Approach.

Journal: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association

Published: September 15, 2025

Real-world effectiveness of highly purified cannabidiol in epilepsy associated with 15q11.2-q13.1 duplication and deletion syndromes: A multicenter study.

Journal: Epilepsia open

Published: September 08, 2025

Early-Onset 15q11.2 Microdeletion Syndrome in a Six-Year-Old Child: A Case Report of Refractory Epilepsy, Autism, and Multisystem Manifestations.

Journal: Cureus

Published: August 19, 2025

Prenatal Diagnosis of MSL2-Related Ventriculomegaly in Association With an Inherited 15q13 Microduplication.

Journal: Clinical genetics

Published: August 11, 2025

15q11.2 Microdeletion Latest Advances

Find the Latest Research About 15q11.2 Microdeletion

Refining the electroclinical phenotype of 15q11.2 microdeletion: EEG biomarker overlap with Angelman syndrome.

Refining the electroclinical phenotype of 15q11.2 microdeletion: EEG biomarker overlap with Angelman syndrome.

The Association of Environmental Variables with Intelligence and Well-Being in Copy Number Variation (CNV) Carriers.

The Association of Environmental Variables with Intelligence and Well-Being in Copy Number Variation (CNV) Carriers.

Prenatal diagnosis and pregnancy outcome of fetuses with 15q11.2 BP1-BP2 microdeletion syndrome: a single-center retrospective study of 34 cases.

Prenatal diagnosis and pregnancy outcome of fetuses with 15q11.2 BP1-BP2 microdeletion syndrome: a single-center retrospective study of 34 cases.

Prenatal diagnosis of familial concomitant 2q11.1q11.2 deletion and 15q11.2 deletion in a pregnancy associated with no apparently phenotypic abnormality.

Prenatal diagnosis of familial concomitant 2q11.1q11.2 deletion and 15q11.2 deletion in a pregnancy associated with no apparently phenotypic abnormality.

Outcomes and Management of Pregnancies Screening Positive for Microdeletions 22q11.2, 15q11.2, 1p36, 4p, or 5p: A Retrospective Cohort Study.

Outcomes and Management of Pregnancies Screening Positive for Microdeletions 22q11.2, 15q11.2, 1p36, 4p, or 5p: A Retrospective Cohort Study.

Genomics of Complex Neurodevelopmental Disorders with Variable Epilepsy Phenotypes: A Clinical Review of Dup15q Syndrome.

Genomics of Complex Neurodevelopmental Disorders with Variable Epilepsy Phenotypes: A Clinical Review of Dup15q Syndrome.

Diagnostic value of karyotyping, CMA/CNV-seq, and WES in fetuses with thickened nuchal translucency: perinatal and two-year follow-up outcomes.

Diagnostic value of karyotyping, CMA/CNV-seq, and WES in fetuses with thickened nuchal translucency: perinatal and two-year follow-up outcomes.

White matter microstructure differences between 15q11.2 copy number variation carriers and non-carriers in mid-to-late life.

White matter microstructure differences between 15q11.2 copy number variation carriers and non-carriers in mid-to-late life.

Simultaneous Le Fort III and Le Fort I Osteotomies for Rare Midfacial Hypoplasia in a Patient with 15q11.2 Microdeletion-A Multidisciplinary Approach.

Simultaneous Le Fort III and Le Fort I Osteotomies for Rare Midfacial Hypoplasia in a Patient with 15q11.2 Microdeletion-A Multidisciplinary Approach.

Real-world effectiveness of highly purified cannabidiol in epilepsy associated with 15q11.2-q13.1 duplication and deletion syndromes: A multicenter study.

Real-world effectiveness of highly purified cannabidiol in epilepsy associated with 15q11.2-q13.1 duplication and deletion syndromes: A multicenter study.

Early-Onset 15q11.2 Microdeletion Syndrome in a Six-Year-Old Child: A Case Report of Refractory Epilepsy, Autism, and Multisystem Manifestations.

Early-Onset 15q11.2 Microdeletion Syndrome in a Six-Year-Old Child: A Case Report of Refractory Epilepsy, Autism, and Multisystem Manifestations.

Prenatal Diagnosis of MSL2-Related Ventriculomegaly in Association With an Inherited 15q13 Microduplication.

Prenatal Diagnosis of MSL2-Related Ventriculomegaly in Association With an Inherited 15q13 Microduplication.