Peer-reviewedCC BYMolecular genetics & genomic medicine
Newborn Screening of Primary Carnitine Deficiency and Prenatal Genetic Diagnosis for a Recurrence‐Risk Family
- 1Yancheng Maternal and Child Health Care Hospital Affiliated to Yangzhou University
Related
- Prenatal ultrasound diagnosis of harlequin ichthyosis: A rare congenital skin disorder
- Prenatal Diagnosis and Postnatal Follow‐Up of 19 Fetuses With 16p13.11 Microduplication in a Cohort of 12,038 Pregnancies From South Zhejiang
- Fraser Syndrome From Prenatal Diagnosis to Multidisciplinary Management and Long-Term Care: A Narrative Review.
- Molecular Genetic Analysis and Prenatal Diagnosis of a Family With MECP2 Duplication Syndrome.
- Prenatal diagnosis of Fowler syndrome with two novel pathogenic variants of FLVCR2
BibTeX
@article{sun2026newborn,
title = {{Newborn Screening of Primary Carnitine Deficiency and Prenatal Genetic Diagnosis for a Recurrence‐Risk Family}},
author = {Huilin Sun and Jianli Zheng and Chong Zhou and Haihong Chen and Lu Zhang and Xiaorui Li and Daocheng Bao and Fangfang Yang and Jianbing Liu},
journal = {Molecular genetics \& genomic medicine},
year = {2026},
month = oct,
url = {https://europepmc.org/article/PMC/PMC13655303},
note = {CC BY},
}
RIS
TY - JOUR
TI - Newborn Screening of Primary Carnitine Deficiency and Prenatal Genetic Diagnosis for a Recurrence‐Risk Family
AU - Huilin Sun
AU - Jianli Zheng
AU - Chong Zhou
AU - Haihong Chen
AU - Lu Zhang
AU - Xiaorui Li
AU - Daocheng Bao
AU - Fangfang Yang
AU - Jianbing Liu
PY - 2026
DA - 2026/10/01
JO - Molecular genetics & genomic medicine
UR - https://europepmc.org/article/PMC/PMC13655303
SN - 2324-9269
ER -