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THE ROLE OF PREIMPLANTATION GENETIC DIAGNOSIS FOR RISK REDUCTION OF PREGNANCY LOSSES IN PATIENTS WITH BALANCED CHROMOSOME REARRANGEMENTS
ANDRONOVA N., ZARETSKAYA N., KHODZHEVA Z., DORONINA O., BYKOVSKAYA O., RUTMAN B., YUTKIN E., YAKOVENKO S.
USE OF PREIMPLANTATION DIAGNOSIS WITHIN THE FRAMEWORK OF AN ASSISTED REPRODUCTIVE TECHNOLOGY PROGRAM FOR MARRIED COUPLES WITH A COMBINATION OF MUTATIONS AT THE AZF LOCUS OF THE Y CHROMOSOME AND CFTR GENE POLYMORPHISM IN HUSBANDS
BELYAEVA N., GLINKINA Z., SOKUR S., GUBAYEVA Z., DOLGUSHINA N., KALININIA E.
Cardiac pathology in cases of monozygotic twins with chromosome 22 deletion syndrome (22q11DS)
Yarygina T., Gasanova R., Bolshakova A., Marzoeva O., Sypchenko E., Gus A.
A noninvasive prenatal test in the diagnosis of chromosome aneuploidies
Kurtser M., Gnetetskaya V.
Diagnosis of male infertility associated with microdeletions at the AZF locus of the Y chromosome
Barkov I., Soroka N., Popova A., Gamidov S., Belyaeva N., Glinkina Z., Kalinina E., Trofimov D., Sukhikh G.
PLACENTAL PATHOLOGY IN FETAL CHROMOSOME ABNORMALITIES
ANDRONOVA N., ZARETSKAYA N., KHODZHAEVA Z., SHCHEGOLEV A., KHRAMCHENKO N., VOEVODIN S.
RISK OF CONGENITAL FETAL ANOMALIES IN THE CARRIERS OF BALANCED CHROMOSOME REARRANGEMENTS AFTER DIFFERENT CONCEPTION PROCEDURES
ANDRONOVA N., ZARETSKAYA N., KHODZHAYEVA Z., DORONINA O., BYKOVSKAYA O., YAKOVENKO S.
PRESENTATION OF NONRANDOM X CHROMOSOME INACTIVATION AND ANDROGEN RECEPTOR GENE POLYMORPHISM IN DIFFERENT PHENOTYPES OF POLYCYSTIC OVARY SYNDROME
CHERNUKHA G., NEMOVA Y., BLINOVA I., RUDENKO V.
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