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1دورية أكاديمية
المؤلفون: Tosca, L, Giltay, J C, Bouvattier, C, Klijn, A J, Bouligand, J, Lambert, A S, Lecerf, L, Josso, N, Tachdjian, G, Picard, J Y
المساهمون: Child Health, Genetica Klinische Genetica, Urologie Medisch Kinderen, Other research (not in main researchprogram)
مصطلحات موضوعية: AMH receptor type 2, anti-Müllerian hormone, disorders of sex development, microdeletion, mutation, persistent Müllerian duct syndrome, Reproductive Medicine, Obstetrics and Gynaecology
وصف الملف: application/pdf
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2دورية أكاديمية
المؤلفون: Tarnow, L, Parving, H H, Jacobsen, P, Rossing, P, Lecerf, L, Poirier, O, Cambien, F
المصدر: Ugeskrift for Laeger. 160(34):4886
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3دورية أكاديمية
المؤلفون: Lecerf, L., Moczar, M., Loisance, D.
المصدر: The Journal of Thoracic and Cardiovascular Surgery ; volume 114, issue 6, page 1117-1118 ; ISSN 0022-5223
مصطلحات موضوعية: Cardiology and Cardiovascular Medicine, Pulmonary and Respiratory Medicine, Surgery
الإتاحة: https://doi.org/10.1016/s0022-5223Test(97)70028-x
https://api.elsevier.com/content/article/PII:S002252239770028X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S002252239770028X?httpAccept=text/plainTest -
4دورية أكاديمية
المؤلفون: Jemaa, R, Fumeron, F, Poirier, O, Lecerf, L, Evans, A, Arveiler, D, Luc, G, Cambou, J P, Bard, J M, Fruchart, J C
المصدر: Journal of Lipid Research ; volume 36, issue 10, page 2141-2146 ; ISSN 0022-2275
مصطلحات موضوعية: Cell Biology, Endocrinology, Biochemistry
الإتاحة: https://doi.org/10.1016/s0022-2275Test(20)39198-7
https://api.elsevier.com/content/article/PII:S0022227520391987?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S0022227520391987?httpAccept=text/plainTest -
5دورية أكاديمية
المؤلفون: EVANS, A. E., POIRIER, O., KEE, F., LECERF, L., MCCRUM, E., FALCONER, T., CRANE, J., O'ROURKE, D. F., CAMBIEN, F.
مصطلحات موضوعية: Original papers
وصف الملف: text/html
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6دورية أكاديمية
المؤلفون: Cambien, F, Costerousse, O, Tiret, L, Poirier, O, Lecerf, L, Gonzales, M F, Evans, A, Arveiler, D, Cambou, J P, Luc, G
المصدر: Circulation ; volume 90, issue 2, page 669-676 ; ISSN 0009-7322 1524-4539
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7دورية أكاديمية
المؤلفون: Watanabe, Y, Stanchina, L, Lecerf, L, Gacem, N, Conidi, Andrea, Baral, V, Pingault, V, Huylebroeck, Danny, Bondurand, N
المصدر: Watanabe , Y , Stanchina , L , Lecerf , L , Gacem , N , Conidi , A , Baral , V , Pingault , V , Huylebroeck , D & Bondurand , N 2017 , ' Differentiation of Mouse Enteric Nervous System Progenitor Cells Is Controlled by Endothelin 3 and Requires Regulation of Ednrb by SOX10 and ZEB2 ' , Gastroenterology , vol. 152 , no. 5 , pp. 1139-+ . https://doi.org/10.1053/j.gastro.2016.12.034Test
الإتاحة: https://doi.org/10.1053/j.gastro.2016.12.034Test
https://pure.eur.nl/en/publications/473596ce-a9b2-4b09-8835-d92a012d900fTest
http://hdl.handle.net/1765/98924Test -
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المؤلفون: Katzaki, E, Morin, G, Pollazzon, M, Papa, Ft, Buoni, S, Hayek, J, Andrieux, J, Lecerf, L, Popovici, C, Receveur, A, MATHIEU DRAMARD, M, Renieri, Alessandra, Mari, Francesca, Philip, N., Papa, FILOMENA TIZIANA
المصدر: American Journal of Medical Genetics Part A. :1711-1717
مصطلحات موضوعية: Male, Pediatrics, medicine.medical_specialty, Adolescent, Chromosomes, Human, Pair 21, Platelet disorder, Young Adult, Myelogenous, Pregnancy, Intellectual Disability, hemic and lymphatic diseases, Genetics, Humans, Medicine, Young adult, Child, Genetics (clinical), Comparative Genomic Hybridization, business.industry, Infant, Newborn, Infant, Syndrome, Mild dysmorphic features, medicine.disease, Thrombocytopenia, Developmental disorder, Leukemia, Child, Preschool, Female, Chromosome Deletion, business, Chromosome 21, Comparative genomic hybridization
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f36957cf59dc606b323f87eec71fe8acTest
https://doi.org/10.1002/ajmg.a.33478Test -
9دورية أكاديمية
المؤلفون: KATZAKI E., MORIN G., POLLAZZON M., PAPA F. T., BUONI S., HAYEK J., ANDRIEUX J., LECERF L., POPOVICI C., RECEVEUR A., MATHIEU-DRAMARD M., RENIERI A., MARI F., PHILIP N.
المساهمون: Katzaki, E., Morin, G., Pollazzon, M., Papa, F. T., Buoni, S., Hayek, J., Andrieux, J., Lecerf, L., Popovici, C., Receveur, A., MATHIEU-DRAMARD, M., Renieri, A., Mari, F., Philip, N.
مصطلحات موضوعية: 21q interstitial deletion, Array-CGH, Chromosome 21, Mental retardation, Thrombocytopenia
وصف الملف: STAMPA
العلاقة: info:eu-repo/semantics/altIdentifier/pmid/20578134; info:eu-repo/semantics/altIdentifier/wos/WOS:000280115000043; volume:152A; issue:7; firstpage:1711; lastpage:1717; numberofpages:7; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART A; http://hdl.handle.net/11365/19074Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-77954121027
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10دورية أكاديمية
المؤلفون: Guediche, N., Tosca, L., Kara Terki, A., Bas, C., Lecerf, L., Young, J., Briand-Suleau, A., Tou, B., Bouligand, J., Brisset, S., Misrahi, M., Guiochon-Mantel, A., Goossens, M., Tachdjian, G.
المصدر: Reproductive BioMedicine Online ; volume 24, issue 1, page 72-82 ; ISSN 1472-6483
مصطلحات موضوعية: Developmental Biology, Reproductive Medicine, Obstetrics and Gynecology
الإتاحة: https://doi.org/10.1016/j.rbmo.2011.08.014Test
https://api.elsevier.com/content/article/PII:S1472648311004883?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1472648311004883?httpAccept=text/plainTest