Zobrazeno 1 - 10
of 18
pro vyhledávání: '"L Y, Pylyp"'
Publikováno v:
Regulatory Mechanisms in Biosystems, Vol 4, Iss 1, Pp 14-22 (2013)
Проведено аналіз частот і типів хромосомних аномалій у 724 чоловіків із безпліддям. Аномалії каріотипу виявлено у 48 (6,6%) пацієнтів. Аномал
Externí odkaz:
https://doaj.org/article/acf9938e622943389856e1b33b0f7da4
Publikováno v:
Journal of Stem Cell Therapy and Transplantation. 3:001-008
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::486d5c0094b519e9078eaddf15ebcbbe
https://doi.org/10.29328/journal.jsctt.1001013
https://doi.org/10.29328/journal.jsctt.1001013
Publikováno v:
Cytology and Genetics. 51:268-271
Androgen insensitivity syndrome (AIS) occurs when target tissues are resistant to the effect of androgens resulting in phenotype with varying degrees of feminization ranging from male infertility to completely normal female external genitalia in pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cdcff886926a6a39e7e8d31fd0ce1f32
https://doi.org/10.3103/s0095452717040089
https://doi.org/10.3103/s0095452717040089
Publikováno v:
Cytology and Genetics. 50:339-342
Complex chromosomal rearrangements are rarely observed prenatally. Genetic counceling of CCR carriers is complicated, especially in cases of de novo origin of the rearrangement. Here we present a new case of a de novo CCR involving four chromosomes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::569279bce7c7d6cbcd1185c71c7d50db
https://doi.org/10.3103/s009545271605011x
https://doi.org/10.3103/s009545271605011x
Publikováno v:
TSitologiia i genetika. 50(4)
Complex chromosomal rearrangements are rarely observed prenatally. Genetic counceling of CCR carriers is complicated, especially in cases of de novo origin of the rearrangement. Here we present a new case of a de novo CCR involving four chromosomes o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15755df43dc861a01c570718b42c0d84
https://pubmed.ncbi.nlm.nih.gov/30480420
https://pubmed.ncbi.nlm.nih.gov/30480420
Publikováno v:
Cytology and Genetics. 49:173-177
The results of cytogenetic studies of 3414 patients with infertility (1741 women and 1673 men) were analyzed retrospectively to estimate the frequency and types of chromosomal abnormalities in infertile patients. Chromosomal abnormalities were detect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7af988cb3e05de4530923817fe6bb7dc
https://doi.org/10.3103/s009545271503010x
https://doi.org/10.3103/s009545271503010x
Autor:
Nataliya V. Verhoglyad, Lyudmyla O. Spynenko, V. Zukin, L. Y. Pylyp, Dmytro Mykytenko, Anna O. Mishenko
Publikováno v:
Journal of assisted reproduction and genetics. 35(2)
The purpose of this study is to perform a retrospective analysis of types and frequencies of chromosomal abnormalities detected by conventional cytogenetic studies in first-trimester miscarriages after spontaneous conception and IVF. Standard cytogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::859b95ac19d02b96eda2ff3ec283b84a
https://pubmed.ncbi.nlm.nih.gov/29086320
https://pubmed.ncbi.nlm.nih.gov/29086320
Publikováno v:
Cytology and Genetics. 48:175-179
Meiotic segregation of chromosomes 13 and 14 was assessed by fluorescence in situ hybridization on sperm of five heterozygous carriers of the most frequent Robertsonian translocation der(13;14). Alternate segregation mode was predominant (mean 78.2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::354e42d4587a6c7ac76cfb0a0fa570cf
https://doi.org/10.3103/s0095452714030086
https://doi.org/10.3103/s0095452714030086
Publikováno v:
Cytogenetic and Genome Research. 142:161-166
Balanced chromosomal translocations do not normally have phenotypic manifestation, but lead to increased risk of infertility, miscarriage and live-birth of chromosomally unbalanced offspring in carriers. The risk assessment of such outcomes in carrie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffda2c66d07b53237ef64f1a9b287a97
https://doi.org/10.1159/000357606
https://doi.org/10.1159/000357606
Publikováno v:
Reproductive BioMedicine Online. 36:e22-e23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b4016513a38c9ee09e5c5baffd8c8310
https://doi.org/10.1016/j.rbmo.2017.10.053
https://doi.org/10.1016/j.rbmo.2017.10.053