-
1دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
2
المؤلفون: Chloé Puisney-Dakhli, G Tachdjian, Hanane Bouchghoul, Francesca Gubana, Valérie Gautier, Aline Receveur, Francois Michael Petit, Jelena Martinovic
المصدر: American Journal of Medical Genetics Part A. 185:1494-1497
مصطلحات موضوعية: Alveolar capillary dysplasia, Pathology, medicine.medical_specialty, Fetus, medicine.diagnostic_test, Heart malformation, business.industry, Prenatal diagnosis, medicine.disease, Hypoplastic left heart syndrome, Genetics, medicine, Fetal Examination, business, Increased nuchal translucency, Genetics (clinical), Fluorescence in situ hybridization
-
3دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
4
المؤلفون: Nathalie Massin, Alexandra Benachi, Véronique Drouineaud, G Tachdjian, Céline Chalas, Nelly Frydman, Catherine Patrat, Aline Receveur, Francois Michael Petit
المصدر: Basic and Clinical Andrology, Vol 30, Iss 1, Pp 1-6 (2020)
Basic and Clinical Andrologyمصطلحات موضوعية: Sperm donation, Urology, Population, Germline mosaicism, Chromosomal rearrangement, Biology, Mosaïque germinale, Germline, Don de spermatozoïdes, film.subject, FISH, medicine, Spermatozoïde, Copy-number variation, education, Genetics, education.field_of_study, Pregnancy, lcsh:R5-920, medicine.diagnostic_test, medicine.disease, Spermatozoa, Réarrangement chromosomique, Reproductive Medicine, film, Amniocentesis, lcsh:Medicine (General), Research Article
-
5
المؤلفون: Laure Lecerf, Irina Giurgea, Quitterie Laudouar, Audrey Briand, Sophie Brisset, Solveig Heide, Aurélie Mouka, G Tachdjian, Lionel Van Maldergem, Michel Goossens, Corinne Metay, Loïc Drévillon, Valérie Ortonne, Lucie Tosca, Virginie Benoit
المساهمون: Service d'histologie, embryologie et cytogénétique [Béclère], Université Paris-Sud - Paris 11 (UP11)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-AP-HP - Hôpital Antoine Béclère [Clamart], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Service de Biochimie [Mondor], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Henri Mondor-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), IMRB - 'Biologie du système neuromusculaire' [Créteil] (U955 Inserm - UPEC), École nationale vétérinaire d'Alfort (ENVA)-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)-Institut National de la Santé et de la Recherche Médicale (INSERM)-IFR10-Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Université Paris-Est Créteil Val-de-Marne - Faculté de médecine (UPEC Médecine), Université Paris-Est Créteil Val-de-Marne - Paris 12 (UPEC UP12), Centre de génétique humaine [CHRU Besançon], Centre Hospitalier Régional Universitaire de Besançon (CHRU Besançon), Université Paris-Saclay, AP-HP Hôpital Bicêtre (Le Kremlin-Bicêtre), UF de Génétique Clinique et Centre de Reference Anomalies du Développement et Syndromes Malformatifs, Sorbonne Université (SU), Service de génétique et embryologie médicales [CHU Trousseau], CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Gestionnaire, Hal Sorbonne Université, École nationale vétérinaire - Alfort (ENVA)-Institut Mondor de Recherche Biomédicale (IMRB), Maladies génétiques d'expression pédiatrique [CHU Trousseau] (Inserm U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], UF de Génétique moléculaire [CHU Trousseau]
المصدر: Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Wiley Periodicals, Inc. In press, pp.e1645. ⟨10.1002/mgg3.1645⟩
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)مصطلحات موضوعية: Male, CNTNAP2, Candidate gene, Developmental Disabilities, [SDV]Life Sciences [q-bio], Chromosome Disorders, Haploinsufficiency, QH426-470, Bioinformatics, medicine.disease_cause, Craniofacial Abnormalities, Epilepsy, Holoprosencephaly, KMT2C haploinsufficiency, 7q35q36.1, interstitial deletion, Genetics (clinical), Chromosome 7 (human), 0303 health sciences, Mutation, Clinical Report, 030305 genetics & heredity, Hypotonia, 3. Good health, DNA-Binding Proteins, [SDV] Life Sciences [q-bio], Phenotype, Child, Preschool, array‐CGH, [SDV.BBM.GTP] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Chromosome Deletion, medicine.symptom, CNTNAP2 disruption, Chromosomes, Human, Pair 7, Noninvasive Prenatal Testing, Nerve Tissue Proteins, Clinical Reports, 03 medical and health sciences, [SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN], Genetics, medicine, Humans, Molecular Biology, 030304 developmental biology, business.industry, Membrane Proteins, medicine.disease, array-CGH, business
وصف الملف: application/pdf
-
6دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
7
المؤلفون: G. Tachdjian
المصدر: EMC - Ginecología-Obstetricia. 53:1-11
مصطلحات موضوعية: 0301 basic medicine, 03 medical and health sciences, 030104 developmental biology
-
8دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
9
المؤلفون: Anne Mayeur, Naouel Ahdad, Nelly Frydman, Laetitia Hesters, G Tachdjian, Serge Romana, Sophie Brisset, Lucie Tosca
المساهمون: Université Paris Descartes - Paris 5 (UPD5)
المصدر: Reproductive BioMedicine
Reproductive BioMedicine Online, Elsevier, 2019, 38, pp.46-55. ⟨10.1016/j.rbmo.2018.10.003⟩مصطلحات موضوعية: Adult, Male, [SDV]Life Sciences [q-bio], Robertsonian translocation, Chromosomal translocation, Biology, medicine.disease_cause, Translocation, Genetic, Male infertility, 03 medical and health sciences, Semen quality, 0302 clinical medicine, medicine, Humans, Gene, In Situ Hybridization, Fluorescence, Retrospective Studies, Genetics, Chromosome Aberrations, 0303 health sciences, 030219 obstetrics & reproductive medicine, Sperm Count, urogenital system, 030305 genetics & heredity, Obstetrics and Gynecology, Chromosome, Karyotype, medicine.disease, Sperm, Spermatozoa, Semen Analysis, Reproductive Medicine, Karyotyping, Sperm Motility, Developmental Biology
-
10
المؤلفون: Isabelle Plo, Romain Diot, Marie Cambot, G Tachdjian, Eric Soler, Virginie Dufour, Najet Debili, Zakia Aid, Hana Raslova, Cyril Catelain, Rachel Petermann, Stefania Mazzi, Sébastien Malinge, Yasmine Mammasse, Thomas Mercher, Mathieu Vieira, Elie Robert, Sylvie Souquere, Aurelie Siret, Philippe Rameau, William Vainchenker, Fabien Boudia, Brahim Arkoun
المصدر: Blood. 136:1-1
مصطلحات موضوعية: Acute megakaryoblastic leukemia, Down syndrome, business.industry, Immunology, Cancer research, Medicine, Cell Biology, Hematology, business, medicine.disease, Induced pluripotent stem cell, Biochemistry
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::aa70a6b17bd6b97f8c4d839fb4a552df
https://doi.org/10.1182/blood-2020-140986