लोड हो रहा है...
Cognitive and Adaptive Characterization of Children and Adolescents with KBG Syndrome: An Explorative Study
KBG syndrome (KBGS) is a rare Mendelian condition caused by heterozygous mutations in ANKRD11 or microdeletions in chromosome 16q24.3 encompassing the gene. KBGS is clinically variable, which makes its diagnosis difficult in a significant proportion of cases. The present study aims at delineating th...
में बचाया:
| में प्रकाशित: | J Clin Med |
|---|---|
| मुख्य लेखकों: | , , , , , , , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
MDPI
2021
|
| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8038739/ https://ncbi.nlm.nih.gov/pubmed/33917340 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/jcm10071523 |
| टैग : |
टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!
|