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SUMPh)
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REVISTE MEDICALE NEINSTITUȚIONALE
Buletin de Perinatologie
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Results 1-7 of 7 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2020
Role of medico-genetic counseling and prenatal screening in diagnosis of renal urinary pathology in fetus
Sprincean, Mariana
;
Hadjiu, Svetlana
;
Halabudenco, Elena
;
Fuior, Liliana
;
Racovitsa, Stela
;
Egorov, V.
;
Barbova, Natalia
;
Neamtsu, B.M.L.
;
Neamtsu, M.L.
;
Calcii, Cornelia
;
Revenco, Ninel
2016
Rolul consultului medico-genetic în profilaxia bolilor genetice prin diagnostic citogenetic prenatal
Sprincean, Mariana
;
Barbova, Natalia
;
Uşurelu, Natalia
;
Halabudenco, Elena
;
Eţco, Ludmila
;
Secrieru, Viorica
;
Nour, Veronica
;
Sacara, Victoria
;
Stratila, M.
2012
Particularităţile polimorfismului clinic şi citogenetic în sindromul Turner
Sprincean, Mariana
;
Barbova, Natalia
;
Halabudenco, Elena
;
Mişina, Ana
;
Samoilenco, Tatiana
2014
Sindromul Klinefelter – particularităţile polimorfismului clinic şi citogenetic
Sprincean, Mariana
;
Halabudenco, Elena
;
Barbova, Natalia
;
Mişina, Ana
;
Samoilenco, Tatiana
2022
Bolile genetice cu risc de accident vascular cerebral ischemic la copii
Sprincean, Mariana
;
Hadjiu, Svetlana
;
Calcii, Cornelia
;
Racoviță, Stela
;
Tihai, Olga
;
Popa, Cristina
;
Dumitraș, Aliona
;
Halabudenco, Elena
;
Lupuşor, Nadejda
;
Revenco, Ninel
2013
Particularităţile polimorfismului clinic şi citogenetic în sindromul Turner
Sprincean, Mariana
;
Barbova, Natalia
;
Halabudenco, Elena
;
Mişina, Ana
;
Samoilenco, Tatiana
2013
Oportunităţi şi perspective de diagnostic citogenetic prenatal al sindromului Down în Republica Moldova
Barbova, Natalia
;
Strătilă, Mihail
;
Sprincean, Mariana
;
Egorov, Vladimir
;
Halabudenco, Elena
;
Secrieru, Viorica
Discover
Author
6
Barbova, Natalia
3
Mişina, Ana
3
Samoilenco, Tatiana
2
Calcii, Cornelia
2
Hadjiu, Svetlana
2
Revenco, Ninel
2
Secrieru, Viorica
1
Dumitraș, Aliona
1
Egorov, V.
1
Egorov, Vladimir
.
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Subject
3
diagnosis
2
karyotype
2
medical genetic counseling
2
prenatal cytogenetic diagnosis
2
Turner syndrome
1
children
1
Down syndrome
1
fetus
1
genetic counseling
1
genetic diseases
.
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Date issued
2
2013
1
2012
1
2014
1
2016
1
2020
1
2022
Has File(s)
7
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