Zobrazeno 1 - 6
of 6
pro vyhledávání: '"rapid aneuploidy test"'
Autor:
Sandip C Shah, Nidhi D Shah, Parth S Shah, Hari Shankar P Ray, Ketan K Vaghasia, Anil K Mehta, Bhavini S Shah, Mandava V Rao
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 8, Pp GC05-GC10 (2019)
Introduction: Among all chromosomes (46) in the human genome, particular significance has been given to chromosomes 13, 18, 21, X and Y. This is primarily because of aneuploidy in these chromosomes that result in viable pregnancies with congenital de
Externí odkaz:
https://doaj.org/article/6ad62cd54d394553bd6315391ac261be
Autor:
Mandava V. Rao, Bhavini S Shah, Ketan K Vaghasia, Nidhi D Shah, Sandip C Shah, Hari Shankar P Ray, Parth S Shah, Anil K Mehta
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 8, Pp GC05-GC10 (2019)
Introduction: Among all chromosomes (46) in the human genome, particular significance has been given to chromosomes 13, 18, 21, X and Y. This is primarily because of aneuploidy in these chromosomes that result in viable pregnancies with congenital de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c0d32d43aa8b10b911426e62baced3c
Autor:
Kooper Angelique JA, Pieters Jacqueline JPM, Faas Brigitte HW, Hoefsloot Lies H, van der Burgt Ineke, Zondervan Hans A, Smits Arie PT
Publikováno v:
Molecular Cytogenetics, Vol 5, Iss 1, p 7 (2012)
Abstract As a routine, karyotyping of invasive prenatal samples is performed as an adjunct to referrals for DNA mutation detection and metabolic testing. We performed a retrospective study on 500 samples to assess the diagnostic value of this procedu
Externí odkaz:
https://doaj.org/article/29a5118450074e2390c91fed2a591cb9
Autor:
Arie P. T. Smits, Ineke van der Burgt, Angelique J. A. Kooper, Hans A Zondervan, J. J. P. M. Pieters, Brigitte H. W. Faas, Lies H. Hoefsloot
Publikováno v:
Molecular Cytogenetics, Vol 5, Iss 1, p 7 (2012)
Molecular cytogenetics, 5(1):7. BioMed Central
Molecular Cytogenetics
Molecular cytogenetics, 5(1):7. BioMed Central
Molecular Cytogenetics
As a routine, karyotyping of invasive prenatal samples is performed as an adjunct to referrals for DNA mutation detection and metabolic testing. We performed a retrospective study on 500 samples to assess the diagnostic value of this procedure. These
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad80ac2fe2cc36c43ebb84a711cc17a9
https://doi.org/10.1186/1755-8166-5-7
https://doi.org/10.1186/1755-8166-5-7
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Akademický článek
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