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1.
Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report.
BMC Pediatr
; 18(1): 138, 2018 04 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-29665810
2.
Disruption of TBC1D7, a subunit of the TSC1-TSC2 protein complex, in intellectual disability and megalencephaly.
J Med Genet
; 50(11): 740-4, 2013 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-23687350
3.
Routine Clinically Detected Increased ROS1 Transcripts Are Related With ROS1 Expression by Immunohistochemistry and Associated With EGFR Mutations in Lung Adenocarcinoma.
JTO Clin Res Rep
; 4(7): 100530, 2023 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-37415647
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