Bibliographic Details
| Title: |
Double Genetic Diagnosis Involving MECP2 and EPHB4 in a Child with Neurodevelopmental Delay and Vascular Anomalies: A Case Report. |
| Authors: |
Sanri A; Department of Pediatric Genetics, Samsun Training and Research Hospital, Samsun, Turkey., Mutlu MB; Detagen Genetic Diseases Evaluation Center, Kayseri, Turkey. |
| Source: |
Molecular syndromology [Mol Syndromol] 2025 Oct 23. Date of Electronic Publication: 2025 Oct 23. |
| Publication Type: |
Journal Article |
| Journal Info: |
Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol |
| Database: |
MEDLINE Ultimate |
