Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2019 | 1 |
2021 | 1 |
2024 | 0 |
Search Results
3 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Is the Next Generation Sequencing the Essential Tool for the Early Diagnostic Approach in Congenital Muscular Dystrophy? New Mutation in the Gen LMNA Associated with Serious Phenotype.
Neurol India. 2021 Nov-Dec;69(6):1835-1837. doi: 10.4103/0028-3886.333448.
Neurol India. 2021.
PMID: 34979702
Free article.
The most recurrent monogenic disorders that overlap with the phenotype of Rett syndrome.
Vidal S, Brandi N, Pacheco P, Maynou J, Fernandez G, Xiol C, Pascual-Alonso A, Pineda M; Rett Working Group; Armstrong J.
Vidal S, et al.
Eur J Paediatr Neurol. 2019 Jul;23(4):609-620. doi: 10.1016/j.ejpn.2019.04.006. Epub 2019 May 2.
Eur J Paediatr Neurol. 2019.
PMID: 31105003
Item in Clipboard
Prognostic value of tumoral ploidy in a series of spanish patients with acute lymphoblastic leukemia.
Ramos ML, Palacios JJ, Fournier BG, Martínez JL, Martinez-López J, Conde MC, Izquierdo AM, García MM, Miranda EB.
Ramos ML, et al. Among authors: fournier bg.
Cancer Genet Cytogenet. 2000 Oct 15;122(2):124-30. doi: 10.1016/s0165-4608(00)00290-9.
Cancer Genet Cytogenet. 2000.
PMID: 11106823
Item in Clipboard
Cite
Cite