Newborn genetic screening of congenital adrenal hyperplasia using long-read sequencing

Authors

Yuqi Yang (ORCID: https://orcid.org/0000-0002-7619-9541)
斌张 (ORCID: https://orcid.org/0000-0002-1627-8408)
Bin Yu (ORCID: https://orcid.org/0000-0001-7796-7314)
Ying Wang (ORCID: https://orcid.org/0000-0003-4931-0299)

Institutions

Changzhou No.2 People's Hospital (CN)

Publication Details

Journal: Orphanet Journal of Rare Diseases
Published: 2025-11-21
DOI: https://doi.org/10.1186/s13023-025-04116-1
Primary Topic: Sexual Differentiation and Disorders
Type: article
Field-Weighted Citation Impact: 0.00

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article

Newborn genetic screening of congenital adrenal hyperplasia using long-read sequencing

Yuqi Yang, 斌张, Bin Yu, Ying Wang

Nov 21, 2025

Orphanet Journal of Rare Diseases

Sexual Differentiation and Disorders

article

Newborn genetic screening of congenital adrenal hyperplasia using long-read sequencing

Yuqi Yang, 斌张, Bin Yu, Ying Wang

November 21, 2025article en

Abstract

No abstract available for this paper.

Orphanet Journal of Rare DiseasesVol. 20(1)

Changzhou No.2 People's Hospital (CN)

Openalex Percentile: Top 68%

Sexual Differentiation and Disorders

DOI Open Access PDF OpenAlex

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Newborn genetic screening of congenital adrenal hyperplasia using long-read sequencing — Yuqi Yang, 斌张, et al. · Orphanet Journal of Rare Diseases (2025) | TGRS Research Map | TGRS