Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Birth of a child with trisomy 9 mosaicism syndrome associated with paternal isodisomy 9: case of a positive noninvasive prenatal test result unconfirmed by invasive prenatal diagnosis

Autor: Hong Pan, David S. Cram, Jingmei Ma, Jianguang Zhang, Huixia Yang, Ling Shang

Publikováno v: Molecular Cytogenetics

Background Non-invasive prenatal testing (NIPT) is currently used as a frontline screening test to identify fetuses with common aneuploidies. Occasionally, incidental NIPT results are conveyed to the clinician suggestive of fetuses with rare chromoso

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec2a5ce557910db21274fe8eccae87c2
https://doi.org/10.1186/s13039-015-0145-4

Are there fetal stem cells in the maternal brain?

Autor: Demirhan O., Çekin N., Taştemir D., Tunç E., Güzel A.I., Meral D., Demirbek B.

Fetal cells can enter maternal blood during pregnancy but whether they can also cross the blood-brain barrier to enter the maternal brain remains poorly understood. Previous results suggest that fetal cells are summoned to repair damage to the mother

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______9491::45f88124676c331320f99094703fe3d6
https://hdl.handle.net/20.500.12605/11215

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2-q28 associated with ovarian dysfunction

Autor: Maria Giuseppina Miano, Michele D'Urso, Giorgia Fimiani, Matilde Valeria Ursini, Valerio Ventruto, Geppino Falco, Carmela Laperuta

Publikováno v: Human reproduction (Oxf., Print) 21 (2006): 529–535. doi:10.1093/humrep/dei356
info:cnr-pdr/source/autori:Fimiani G.; Laperuta C.; Falco G.; Ventruto V.; D'Urso M.; Ursini M.V.; Miano M.G./titolo:Heterozygosity mapping by quantitative fluorescent PCR reveals an interstitial deletion in Xq26.2-q28 associated with ovarian dysfunction/doi:10.1093%2Fhumrep%2Fdei356/rivista:Human reproduction (Oxf., Print)/anno:2006/pagina_da:529/pagina_a:535/intervallo_pagine:529–535/volume:21

Background: Deletions of Xq chromosome are reported for a number of familial conditions exhibiting premature ovarian failure (POF) and early menopause (EM). Methods and results: We describe the inheritance of an interstitial deletion of the long arm

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9dc0f6937ae01dcee3a2dfce1dbd079
https://pubmed.ncbi.nlm.nih.gov/16239311