المؤلفون: Issa, Sarah

Thesis Advisors: Paris Est, Pingault, Véronique

مصطلحات موضوعية: Waardenburg, Génétique, Développement, Genetics, Development, 611

الاتاحة: http://www.theses.fr/2017PESC0012

المؤلفون: Dimassi, Hani, Haidar, Suzan, Issa, Sarah, Hassan, Hussein F.

المساهمون: Lebanese American University

المصدر: World Allergy Organization Journal ; volume 13, issue 11, page 100481 ; ISSN 1939-4551

الاتاحة: http://dx.doi.org/10.1016/j.waojou.2020.100481
https://api.elsevier.com/content/article/PII:S1939455120303847?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1939455120303847?httpAccept=text/plain

المؤلفون: Daher, Wajeeh, Omar, Amal, Swaity, Hadeel, Allan, Bushra, Dar Issa, Sarah, Amer, Zahera, Halabi, Aseel

المصدر: Sustainability (2071-1050); Oct2022, Vol. 14 Issue 19, p12865-12865, 11p

المؤلفون: Issa, Sarah, Bondurand, Nadege, Faubert, Emmanuelle, Poisson, Sylvain, Lecerf, Laure, Nitschke, Patrick, Deggouj, Naima, Loundon, Natalie, Jonard, Laurence, David, Albert, Sznajer, Yves, Blanchet, Patricia, Marlin, Sandrine, Pingault, Veronique

المساهمون: UCL - SSS/IONS/NEUR - Clinical Neuroscience, UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Service d'oto-rhino-laryngologie, UCL - (SLuc) Centre de génétique médicale UCL

المصدر: Human Mutation, Vol. 38, no. 5, p. 581-593 (2017)

مصطلحات موضوعية: G protein-coupled receptor, Waardenburg syndrome, endothelin, neurocristopathy

Relation: boreal:184619; http://hdl.handle.net/2078.1/184619; info:pmid/28236341; urn:ISSN:1059-7794; urn:EISSN:1098-1004

الاتاحة: http://hdl.handle.net/2078.1/184619
https://doi.org/10.1002/humu.23206

المؤلفون: Massoud, May A., Issa, Sarah, Fadel, Mutasem El, Jamali, Ibrahim

المصدر: International Journal of Sustainable Society ; volume 8, issue 1, page 54 ; ISSN 1756-2538 1756-2546

الاتاحة: http://dx.doi.org/10.1504/ijssoc.2016.074947

المؤلفون: Issa, Sarah

المساهمون: Annous, Samer, Thesis Advisor

URL الوصول: http://search.shamaa.org/FullRecord?ID=242224

المؤلفون: Mousty, Eve, Issa, Sarah, Grosjean, Frédéric, Col, Jean-Yves, Khau van Kien, Philippe, Perez, Marie-Josée, Petrov, Yuliya, Reboul, Dorothée, Faubert, Emmanuelle, Le Gac, Marie-Pascale, Bondurand, Nadège, Chiesa, Jean, Pingault, Véronique

المساهمون: Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), Institut Mondor de Recherche Biomédicale (IMRB), Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Centre Hospitalier Henri Duffaut (Avignon), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Institut des Biomolécules Max Mousseron [Pôle Chimie Balard] (IBMM), Ecole Nationale Supérieure de Chimie de Montpellier (ENSCM)-Institut de Chimie du CNRS (INC)-Université de Montpellier (UM)-Centre National de la Recherche Scientifique (CNRS), Hôpital Henri Mondor, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Herrada, Anthony

المصدر: Prenatal Diagnosis
Prenatal Diagnosis, 2015, 35 (13), pp.1379-1381. ⟨10.1002/pd.4703⟩
Prenatal Diagnosis, Wiley, 2015, 35 (13), pp.1379-1381. ⟨10.1002/pd.4703⟩

مصطلحات موضوعية: MESH: Waardenburg Syndrome, MESH: Humans, MESH: Pregnancy, [SDV.MHEP] Life Sciences [q-bio]/Human health and pathology, MESH: Young Adult, MESH: Nuchal Translucency Measurement, MESH: PAX3 Transcription Factor, MESH: Paired Box Transcription Factors, MESH: Female, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology, MESH: Homozygote

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1bc257d79efd17617aee2852737e099d
https://hal.umontpellier.fr/hal-03579374

المؤلفون: UCL - SSS/IONS/NEUR - Clinical Neuroscience, UCL - SSS/IREC/SLUC - Pôle St.-Luc, UCL - (SLuc) Service d'oto-rhino-laryngologie, UCL - (SLuc) Centre de génétique médicale UCL, Issa, Sarah, Bondurand, Nadege, Faubert, Emmanuelle, Poisson, Sylvain, Lecerf, Laure, Nitschke, Patrick, Deggouj, Naima, Loundon, Natalie, Jonard, Laurence, David, Albert, Sznajer, Yves, Blanchet, Patricia, Marlin, Sandrine, Pingault, Veronique

المصدر: Human Mutation, Vol. 38, no. 5, p. 581-593 (2017)

مصطلحات الفهرس: G protein-coupled receptor, Waardenburg syndrome, endothelin, neurocristopathy, info:eu-repo/semantics/article

URL: http://hdl.handle.net/2078.1/184619

المؤلفون: Issa, Sarah, Bondurand, Nadege, Faubert, Emmanuelle, Poisson, Sylvain, Lecerf, Laure, Nitschke, Patrick, Deggouj, Naima, Loundon, Natalie, Jonard, Laurence, David, Albert, Sznajer, Yves, Blanchet, Patricia, Marlin, Sandrine, Pingault, Veronique

المصدر: Human Mutation; May2017, Vol. 38 Issue 5, p581-593, 13p