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1.
Imatinib independent aberrant methylation of NOV/CCN3 in chronic myelogenous leukemia patients: a mechanism upstream of BCR-ABL1 function?
Cell Commun Signal
; 17(1): 38, 2019 04 23.
Artículo
en Inglés
| MEDLINE | ID: mdl-31014357
2.
Frequencies of Six (Five Novel) STR Markers Linked to TUSC3 (MRT7) or NSUN2 (MRT5) Genes Used for Homozygosity Mapping of Recessive Intellectual Disability.
Clin Lab
; 61(8): 925-32, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26427135
3.
Molecular Characterization of KRAS, BRAF, and EGFR Genes in Cases with Prostatic Adenocarcinoma; Reporting Bioinformatics Description and Recurrent Mutations.
Clin Lab
; 61(7): 749-59, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-26299074
4.
Development and validation of a novel panel of 16 STR markers for simultaneous diagnosis of ß-thalassemia, aneuploidy screening, maternal cell contamination detection and fetal sample authenticity in PND and PGD/PGS cases.
Sci Rep
; 9(1): 7452, 2019 05 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-31092881
5.
Revisiting a Complex Rearrangement Involving a 619 Base Pairs Deletion, 6 Nucleotide Insertion Followed by a A > G Substitution Causing ß°-Thalassemia.
Indian J Hematol Blood Transfus
; 32(4): 500-503, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27812264
6.
Identification of six novel mutations in Iranian patients with maple syrup urine disease and their in silico analysis.
Mutat Res
; 786: 34-40, 2016 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-26901124
7.
Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3.
Eur J Hum Genet
; 19(1): 115-7, 2011 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-20700148
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