Á lódáil...
A New Case of an Extremely Rare 3p21.31 Interstitial Deletion
Interstitial 3p21.31 deletions have been very rarely reported. We describe a 7-year-old boy with global developmental delay, specific facial characteristics, hydronephrosis, and hypothyreosis with a de novo deletion of 3p21.31, encompassing 29 OMIM genes. Despite the wide use of microarrays, no simi...
Na minha lista:
| Foilsithe in: | Mol Syndromol |
|---|---|
| Main Authors: | , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
S. Karger AG
2016
|
| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4906427/ https://ncbi.nlm.nih.gov/pubmed/27385966 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000445227 |
| Clibeanna: |
Cuir Clib Leis
Gan Chlibeanna, Bí ar an gcéad duine leis an taifead seo a chlibeáil!
|