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46,XX DSD: Developmental, Clinical and Genetic Aspects.
Alkhzouz C, Bucerzan S, Miclaus M, Mirea AM, Miclea D. Alkhzouz C, et al. Among authors: bucerzan s. Diagnostics (Basel). 2021 Jul 30;11(8):1379. doi: 10.3390/diagnostics11081379. Diagnostics (Basel). 2021. PMID: 34441313 Free PMC article. Review.
Diagnostic Usefulness of MLPA Techniques for Recurrent Copy Number Variants Detection in Global Developmental Delay/Intellectual Disability.
Miclea D, Szucs A, Mirea A, Stefan DM, Nazarie F, Bucerzan S, Lazea C, Grama A, Pop TL, Farcas M, Zaharie G, Matyas M, Mager M, Vintan M, Popp R, Alkhzouz C. Miclea D, et al. Among authors: bucerzan s. Int J Gen Med. 2021 Aug 16;14:4511-4515. doi: 10.2147/IJGM.S320033. eCollection 2021. Int J Gen Med. 2021. PMID: 34429637 Free PMC article.
Genetic testing in pediatric endocrine pathology.
Miclea D, Alkhzouz C, Bucerzan S, Grigorescu-Sido P. Miclea D, et al. Among authors: bucerzan s. Med Pharm Rep. 2021 Aug;94(Suppl No 1):S15-S18. doi: 10.15386/mpr-2220. Epub 2021 Aug 10. Med Pharm Rep. 2021. PMID: 34527901 Free PMC article.
23 results