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1.
[Molecular genetics in diagnosis of Coats disease: combination of oligogenic variants associated with different forms of hereditary retinal dystrophy]. / Molekulyarno-geneticheskie nakhodki pri diagnostike bolezni Koatsa: sochetanie oligolokusnykh izmenenii, svyazannykh s raznymi nozologicheskimi formami nasledstvennoi retinopatii.
Vestn Oftalmol;
139(1): 69-74, 2023.
Artículo
en Ruso
| MEDLINE | ID: mdl-36924516
2.
[BRAF-positive paucicellular variant of anaplastic carcinoma in the presence of tall cell variant papillary thyroid cancer]. / BRAF-pozitivnyi malokletochnyi variant anaplasticheskoi kartsinomy na fone papilliarnogo raka shchitovidnoi zhelezy iz vysokikh kletok.
Arkh Patol;
79(3): 27-33, 2017.
Artículo
en Ruso
| MEDLINE | ID: mdl-28631713
3.
SNP-Based Chromosomal Microarray Analysis for Detecting DNA Copy Number Variations in Fetuses with a Thickened Nuchal Fold.
Sovrem Tekhnologii Med;
13(6): 72-76, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-35265361
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