Medicine
 |
|
18 march 2019 23:04:24 |
| Familial inheritance of the 3q29 microdeletion syndrome: case report and review (BMC Medical Genomics) |
|
Tweet The chromosome 3q29 microdeletion syndrome is characterized by a clinical phenotype that includes behavioral features consistent with autism and attention deficit hyperactivity disorder, mild to moderate devel... |
| 83 viewsCategory: Genomics, Medicine |
 BasePhasing: a highly efficient approach for preimplantation genetic haplotyping in clinical application of balanced translocation carriers (BMC Medical Genomics)Analyzing the 3D chromatin organization coordinating with gene expression regulation in B-cell lymphoma (BMC Medical Genomics) 
|
| blog comments powered by Disqus |
MyJournals.org
The latest issues of all your favorite science journals on one page
The latest issues of all your favorite science journals on one page
