Genetic Insights Into Craniosynostosis: Identification of Novel IL11RA Variants in Chinese Pediatric Patients.
- Published in:
- Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 5, p. 1, doi. 10.1002/mgg3.70106
- By:
- Publication type:
- Article
Works matching IS 23249269 AND DT 2025 AND VI 13 AND IP 5
Results: 8
1
2
Correction to "A New Case of Sodium‐Dependent Multivitamin Transporter Defect Occurring as a Life‐Threatening Condition Responsive to Early Vitamin Supplementation and Literature Review".
- Published in:
- 2025
- Publication type:
- Correction Notice
3
Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion Syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 5, p. 1, doi. 10.1002/mgg3.70104
- By:
- Publication type:
- Article
4
Identification and Functional Analysis of Novel Mutations in AXIN2 and LRP6 Linked With Non‐Syndromic Tooth Agenesis.
- Published in:
- Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 5, p. 1, doi. 10.1002/mgg3.70101
- By:
- Publication type:
- Article
5
Functional Correlation of Two Novel Nonsense POU4F3 Mutations Causing Late‐Onset Progressive Nonsyndromic Hearing Loss in DFNA15 Families.
- Published in:
- Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 5, p. 1, doi. 10.1002/mgg3.70100
- By:
- Publication type:
- Article
6
A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene.
- Published in:
- 2025
- By:
- Publication type:
- Case Study
7
Issue Information.
- Published in:
- Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 5, p. 1, doi. 10.1002/mgg3.2458
- Publication type:
- Article
8
Knowledge, Attitudes, and Practices of the General Population Regarding Peripheral Blood Chromosomal Testing in the Premarital or Preconception Context.
- Published in:
- Molecular Genetics & Genomic Medicine, 2025, v. 13, n. 5, p. 1, doi. 10.1002/mgg3.70103
- By:
- Publication type:
- Article