Zobrazeno 1 - 10
of 337
pro vyhledávání: '"Gillerot Y"'
Autor:
Busby, A, Abramsky, L, Dolk, H, Armstrong, B, Addor, MC, Anneren, G, Armstrong, N, Baguette, A, Barisic, [No Value], Berghold, A, Bianca, S, Braz, P, Calzolari, E, Christiansen, M, Cocchi, G, Daltveit, AK, De Walle, H, Edwards, G, Gatt, M, Gener, B, Gillerot, Y, Gjergja, R, Goujard, J, Haeusler, M, Latos-Bielenska, A, McDonnell, R, Neville, A, Olars, B, Portillo, [No Value], Ritvanen, A, Robert-Gnansia, E, Rosch, C, Scarano, G, Steinbicker, [No Value]
Publikováno v:
Reproductive Toxicology, 21(1), 116-116. HANLEY & BELFUS-ELSEVIER INC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::9309b72a85aea658d6e1c17e39652495
https://research.rug.nl/en/publications/5c5e5835-1239-46a2-bceb-e84ff86bbb9c
https://research.rug.nl/en/publications/5c5e5835-1239-46a2-bceb-e84ff86bbb9c
Publikováno v:
Leukemialymphoma. 46(10)
Follicular Lymphoma is a low grade malignancy of mature B-cells. The hallmark chromosome abnormality is the translocation t(14;18) which is observed in 70 – 80% of cases with a translocation t(3;14) present in a further 10%. Rarely both of these tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c6b1776bd1fb30072d18b808a033ebc
https://pubmed.ncbi.nlm.nih.gov/16194898
https://pubmed.ncbi.nlm.nih.gov/16194898
Autor:
Garne, Ester, Loane, M., Dolk, H., De Vigan, C., Scarano, G., Tucker, D., Stoll, C., Gener, B., Pierini, A., Nelen, V., Rosch, C., Gillerot, Y., Feijoo, M., Tincheva, R., Queisser-Luft, A., Addor, M.C., Mosquera, C., Gatt, M., Barisic, I.
Publikováno v:
Garne, E, Loane, M, Dolk, H, De Vigan, C, Scarano, G, Tucker, D, Stoll, C, Gener, B, Pierini, A, Nelen, V, Rosch, C, Gillerot, Y, Feijoo, M, Tincheva, R, Queisser-Luft, A, Addor, M C, Mosquera, C, Gatt, M & Barisic, I 2005, ' Prenatal diagnosis of severe structural congenital malformations in Europe. ', Ultrasound in Obstetrics & Gynecology, vol. 25, no. 1, pp. 6-11 . https://doi.org/10.1002/uog.1784
To assess at a population-based level the frequency with which severe structural congenital malformations are detected prenatally in Europe and the gestational age at detection, and to describe regional variation in these indicators. In the period 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2ec55f7aafffcec83a3cc1f3de6a18d6
https://doi.org/10.1002/uog.1784
https://doi.org/10.1002/uog.1784
Autor:
Garne, Ester, Loane, M., de Vigan, C., Scarano, G., de Walle, H., Gillerot, Y., Stoll, Claude, Addor, Marie-Claude, Stone, David, Gener, Blanca, Feijoo, Maria, Mosquera-Tenreiro, Carmen, Gatt, Miriam, Queisser-Luft, Annette, Baena, Neus, Dolk, Helen
Publikováno v:
Garne, E, Loane, M, de Vigan, C, Scarano, G, de Walle, H, Gillerot, Y, Stoll, C, Addor, M-C, Stone, D, Gener, B, Feijoo, M, Mosquera-Tenreiro, C, Gatt, M, Queisser-Luft, A, Baena, N & Dolk, H 2004, ' Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 registries in Europe ', Prenatal Diagnosis, vol. 24, no. 11, pp. 908-912 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::226aa0cff952478d96687af297d1640b
https://portal.findresearcher.sdu.dk/da/publications/563be040-ed9b-11db-821c-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/563be040-ed9b-11db-821c-000ea68e967b
Akademický článek
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Autor:
Cornel, Mc, Breed, Tenkate, Lpl, Mantingh, A, Ayme, S, Becker, R, Bianchi, F, Calzolari, E, Clementi, Maurizio, Cuschieri, A, Garne, E, Gillerot, Y, Goujard, J
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3657::25a25eddb76099ed3ad72e18c4fa249d
http://hdl.handle.net/11577/2500154
http://hdl.handle.net/11577/2500154
Autor:
Jc, Lapière, Alain VERLOES, Herens C, Delfortrie J, Van Maldergem L, Gillerot Y, Koulischer L
Publikováno v:
Europe PubMed Central
We report a severely mentally retarded, dysmorphic girl aged 7 years with a 47,XX, +der(18), t(10;18)(p11.2;q11.2)mat. The phenotype of our patient is compared with 6 cases of trisomy 10p and 10 cases of trisomy 18q- from the literature. The short tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e716fb97701b1a7f8422c7ccff6535b1
https://pubmed.ncbi.nlm.nih.gov/1388935
https://pubmed.ncbi.nlm.nih.gov/1388935
Autor:
van Maldergem, L., Espeel, M., Wanders, R. J., Roels, F., Gerard, P., Scalais, E., Mannaerts, G. P., Casteels, M., Gillerot, Y.
Publikováno v:
Neuromuscular disorders, 2(3), 217-224. Elsevier Limited
In this paper, we describe a baby male born to healthy non-consanguineous parents presenting at birth with hypotonia and seizures. Additional salient clinical features included the development of glaucoma, the absence of significant facial dysmorphis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=narcis______::50d41033f9b01d0c0ae8f6eabf5386cb
https://pure.amc.nl/en/publications/neonatal-seizures-and-severe-hypotonia-in-a-male-infant-suffering-from-a-defect-in-peroxisomal-betaoxidation(6c8de865-c8b3-4716-953f-36517cc1779a).html
https://pure.amc.nl/en/publications/neonatal-seizures-and-severe-hypotonia-in-a-male-infant-suffering-from-a-defect-in-peroxisomal-betaoxidation(6c8de865-c8b3-4716-953f-36517cc1779a).html
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
A newborn male presenting with a peculiar appearance, hypertonia, a flexum attitude, hypospadias and skeletal abnormalities was found to bear a r 9 chromosome. A phenotypic distinction between early and late presenting forms is discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::45dd52675be61f1ff3a8e7de7d6c3602
https://pubmed.ncbi.nlm.nih.gov/1781957
https://pubmed.ncbi.nlm.nih.gov/1781957
Akademický článek
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