טוען...
Array Comparative Genomic Hybridization (aCGH) Analysis in Prader–Willi Syndrome
Prader–Willi syndrome (PWS) is due to loss of paternally expressed genes in the 15q11–q13 region generally from a paternal 15q11–q13 deletion. The proximal deletion breakpoint in the 15q11–q13 region occurs at one of two sites located within either of two large duplicons allowing for identification...
שמור ב:
| הוצא לאור ב: | Am J Med Genet A |
|---|---|
| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2008
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5438264/ https://ncbi.nlm.nih.gov/pubmed/18266248 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.32249 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|