about
Combined NGS approaches identify mutations in the intraflagellar transport gene IFT140 in skeletal ciliopathies with early progressive kidney DiseaseSerbian high-risk families: extensive results on BRCA mutation spectra and frequency.Polymorphisms in cancer susceptibility genes XRCC1, RAD51 and TP53 and the risk of breast cancer in Serbian women.Novel BRCA1 splice-site mutation in ovarian cancer patients of Slavic origin.Identifying and testing for hereditary susceptibility to breast/ovarian cancer in Serbia: Where are we now?RAD51 135G>C and TP53 Arg72Pro polymorphisms and susceptibility to breast cancer in Serbian womenTherapeutic and Endocrine Effects of Decapeptyl®, Synthetic LH-RH Agonistic Analogue in Premenopausal Women with Metastatic Breast Cancer
P50
Q24318295-4CE09BC4-8C5D-4C32-9C0D-AFB4B71161D2Q46055330-4C07616D-2122-4394-AC5E-028DD725127CQ47863122-ADC7D0C4-D369-45D6-9221-D004FD0CEF3AQ48163026-3F170037-F591-4E7C-9EEE-55C2359D6F71Q57728299-E97E5A00-932C-43B3-B08F-234751A7D2D6Q58886632-CD43BE81-3327-4273-BD15-39A350044E0FQ58886660-84C0222A-A907-4D83-9A77-E73C55F4EC3B
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0001-8751-1281
@en
name
Mirjana Brankovic-Magic
@ast
Mirjana Brankovic-Magic
@en
Mirjana Brankovic-Magic
@es
Mirjana Brankovic-Magic
@nl
type
label
Mirjana Brankovic-Magic
@ast
Mirjana Brankovic-Magic
@en
Mirjana Brankovic-Magic
@es
Mirjana Brankovic-Magic
@nl
prefLabel
Mirjana Brankovic-Magic
@ast
Mirjana Brankovic-Magic
@en
Mirjana Brankovic-Magic
@es
Mirjana Brankovic-Magic
@nl
P106
P1153
55886308600
P31
P496
0000-0001-8751-1281