Zobrazeno 1 - 10
of 67
pro vyhledávání: '"C, Rouillac"'
Autor:
Bérénice Hervé, François Vialard, Justine Besseau-Ayasse, C. Rouillac-Le Sciellour, C. Oheix, D. Molina-Gomes
Publikováno v:
Gynécologie Obstétrique Fertilité & Sénologie. 45:45-49
Publikováno v:
Gynecologie, obstetrique, fertilitesenologie. 45(1)
Publikováno v:
Gynécologie Obstétrique & Fertilité. 36:200-203
Non invasive fetal RhD genotyping, based on polymerase-chain-reaction (PCR), is an accurate and validated technique. It allows a reduction by one-third of anti-D immunoglobulin injections to prevent RhD allo-immunization. In case of maternal anti-D i
Autor:
C. Rouillac-Le Sciellour, Yves Colin, C. Le Van Kim, Y. Brossard, J.-P. Cartron, Y. Guidicelli, Valérie Serazin, O. Oudin, M. Menu
Publikováno v:
Transfusion Clinique et Biologique. 14:572-577
Fetal RHD genotyping from maternal plasma was performed by real-time PCR amplification of exons 7 and 10 of the RHD gene and the amplified products were detected either with SYBR Green I dye according to our previously published method [Mol Diagn 8 (
Autor:
M. Dakouane-Giudicelli, François Vialard, Jacqueline Selva, N. Ledee, Yves Giudicelli, Valérie Serazin, C. Rouillac-Le Sciellour, M. Bergere, Olivier Cussenot, Martine Albert
Publikováno v:
Gynécologie Obstétrique & Fertilité. 34:855-859
The effect of maternal age on the risk of meiotic abnormality is well documented. In contrast little is known about the effect of the paternal age. The question of the risk related to paternal age is raised because of the increased demand of Assisted
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
M. Abitbol, Cécile Marsac, J. M. Saudubray, C Rouillac, C Benelli, Yves Dumez, Françoise Fouque, G. Lindsay, Bernard Aral, Jean-Louis Dufier, Dominique Marchant
Publikováno v:
Prenatal Diagnosis. 19:1160-1164
We have previously reported a genetic study of a neonatal lactic acidosis linked to a pyruvate dehydrogenase complex deficiency due to the absence of the protein X subunit. This rare autosomal recessive disorder is associated with specific deletions
Publikováno v:
Blood. 87:4853-4861
The RH blood group locus is composed of two sequence-related genes, RHD and RHCE, encoding the D, Cc, and Ee antigens in common Rh-positive phenotypes. In this report, we have analyzed the molecular basis of Rh antigens expression in weak D (Du) and
Publikováno v:
Transfusion Clinique et Biologique. 3:497-503
Tentative model for the mapping of D epitopes on the RhD polypeptide The partial D phenotypes correspond to D-positive individuals that may develop anti-D antibodies following immunization by transfusion or pregnancy, since they lack some of the D ep
Autor:
Marylise Beolet, AM D'Ambrosio, Yves Colin, J P Cartron, C Rouillac, C. Le Van Kim, NC Hughes-Jones
Publikováno v:
Blood. 85:2937-2944
The RH blood group locus from RhD-positive donors is composed of two closely related genes, RHCE and RHD, encoding the Cc/Ee and D antigens, respectively. The major Rh antigen, D, is serologically defined as a mosaic of at least nine determinants (ep