A Witteveen-Kolk Syndrome Patient with Reflux Disease and a de novo Deletion of the SIN3A Gene.
Saved in:
| Title: | A Witteveen-Kolk Syndrome Patient with Reflux Disease and a de novo Deletion of the SIN3A Gene. |
|---|---|
| Authors: | Uctepe E; Acibadem Ankara Tissue Typing Laboratory, Ankara, Turkey., Kandemir N; Medical Genetics, Kayseri City Training and Research Hospital, Kayseri, Turkey., Bir FD; Medical Genetics, Ankara Etlik City Training and Research Hospital, Ankara, Turkey., Karhan AN; Pediatric Gastroenterology, Hepatology and Nutrition, Ankara Etlik City Training and Research Hospital, Ankara, Turkey., Tumer S; Acıbadem Labgen Genetic Diagnosis Center, Istanbul, Turkey., Ondes EB; Acıbadem Labgen Genetic Diagnosis Center, Istanbul, Turkey., Konuskan B; Department of Pediatric Neurology, Ankara Etlik City Training and Research Hospital, Ankara, Turkey., Yesilyurt A; Acıbadem Labgen Genetic Diagnosis Center, Istanbul, Turkey.; Acıbadem Maslak Hospital, Istanbul, Turkey. |
| Source: | Molecular syndromology [Mol Syndromol] 2024 Jun; Vol. 15 (3), pp. 251-256. Date of Electronic Publication: 2024 Jan 30. |
| 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 Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
|
Full text is not displayed to guests.
Login for full access.
|
|
| ISSN: | 1661-8769 |
|---|---|
| DOI: | 10.1159/000536072 |
