Broadening the phenotypic and genetic spectrum of ERBB2-associated multisystem congenital disorder

Authors

Birutė Burnytė (ORCID: https://orcid.org/0000-0002-5845-1045)
Aušra Morkūnienė (ORCID: https://orcid.org/0009-0006-1789-5973)
Gabija Gurskaitė (ORCID: https://orcid.org/0009-0006-3926-6529)
Agnė Jakubėnaitė

Institutions

Vilnius University (LT)
Vilnius University Hospital Santariskiu Klinikos (LT)

Publication Details

Journal: BMC Pediatrics
Published: 2026-10-05
DOI: https://doi.org/10.1186/s12887-026-07773-8
Primary Topic: Congenital limb and hand anomalies
Type: article
Field-Weighted Citation Impact: 0.00

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article

Broadening the phenotypic and genetic spectrum of ERBB2-associated multisystem congenital disorder

Birutė Burnytė, Aušra Morkūnienė, Gabija Gurskaitė, Agnė Jakubėnaitė

Oct 5, 2026

BMC Pediatrics

Congenital limb and hand anomalies

article

Broadening the phenotypic and genetic spectrum of ERBB2-associated multisystem congenital disorder

Birutė Burnytė, Aušra Morkūnienė, Gabija Gurskaitė, Agnė Jakubėnaitė

October 5, 2026article en

Abstract

No abstract available for this paper.

BMC Pediatrics

Vilnius University (LT), Vilnius University Hospital Santariskiu Klinikos (LT)

Openalex Percentile: Top 13%

Congenital limb and hand anomalies

DOI Open Access PDF OpenAlex

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Broadening the phenotypic and genetic spectrum of ERBB2-associated multisystem congenital disorder — Birutė Burnytė, Aušra Morkūnienė, et al. · BMC Pediatrics (2026) | TGRS Research Map | TGRS