المؤلفون: Nastasia Cardone, Valentina Taglietti, Serena Baratto, Kaouthar Kefi, Baptiste Periou, Ciryl Gitiaux, Christine Barnerias, Peggy Lafuste, France Leturcq Pharm, Juliette Nectoux Pharm, Chiara Panicucci, Isabelle Desguerre, Claudio Bruno, François-Jerome Authier, Chiara Fiorillo, Frederic Relaix, Edoardo Malfatti

المصدر: Acta Neuropathologica Communications, Vol 11, Iss 1, Pp 1-11 (2023)

مصطلحات موضوعية: Duchenne muscular dystrophy, Fibrosis, FAPs, Muscle regeneration, Cellular senescence, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2051-5960

URL الوصول: https://doaj.org/article/b6d306702c484b0da14b8cd7bffee00a

المؤلفون: Mathilde Pacault, Camille Verebi, Magali Champion, Lucie Orhant, Alexandre Perrier, Emmanuelle Girodon, France Leturcq, Dominique Vidaud, Claude Férec, Thierry Bienvenu, Romain Daveau, Juliette Nectoux

المصدر: PLoS ONE, Vol 18, Iss 4 (2023)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124834/?tool=EBI; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/f019b4efaf6d41fd90675869d221742b

المؤلفون: Laïla Allach El Khattabi, Christelle Rouillac-Le Sciellour, Dominique Le Tessier, Armelle Luscan, Audrey Coustier, Raphael Porcher, Rakia Bhouri, Juliette Nectoux, Valérie Sérazin, Thibaut Quibel, Laurent Mandelbrot, Vassilis Tsatsaris, François Vialard, Jean-Michel Dupont

المصدر: PLoS ONE, Vol 11, Iss 5, p e0155009 (2016)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC4864235?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/4c74b227089a4ed5b2456ee800e56f04

المؤلفون: Guérémy, Alexandre, Salort-Campana, Emmanuelle, Fortanier, Etienne, Magot, Armelle, Bouhour, Françoise, Solé, Guilhem, Noury, Jean-Baptiste, Behin, Anthony, France, Leturcq, Stojkovic, Tanya, du Closel, Luce Barbat, Sacconi, Sabrina, Metay, Corinne, Gorokhova, Svetlana, Attarian, Shahram, Nadaj-pakleza, Aleksandra, Cerino, Mathieu, Eymard, Bruno, Juliette, Nectoux

المصدر: Revue Neurologique ; volume 180, page S117 ; ISSN 0035-3787

الاتاحة: http://dx.doi.org/10.1016/j.neurol.2024.02.227
https://api.elsevier.com/content/article/PII:S0035378724002534?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0035378724002534?httpAccept=text/plain

المؤلفون: Camille Verebi, Roseline Caumes, Sandra Chantot-Bastaraud, Nathalie Deburgrave, Lucie Orhant, Nicolas Vaucouleur, Laurence Cuisset, Thierry Bienvenu, France Leturcq, Juliette Nectoux

المصدر: Neuromuscular Disorders. 33:367-370

مصطلحات موضوعية: Neurology, Pediatrics, Perinatology and Child Health, Neurology (clinical), Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b081ce29fce2cba3f3ba3c5208e4a057
https://doi.org/10.1016/j.nmd.2023.03.004

المؤلفون: Yosra Lajmi, Laurence Loeuillet, Giulia Petrilli, Charles Egloff, Juliette Nectoux, Clémence Molac, Nathalie Roux, Emmanuelle Pannier, Amale Achaiaa, Zaina Ait Arkoub, Sophie Chuon, Aurélie Coussement, Jean Michel Dupont, Valérie Malan, Emmanuel Spaggiari, Ferechte Razavi, Jeanne Amiel, Bettina Bessières, Sarah Grotto, Tania Attié‐Bitach

المصدر: Birth Defects Research. 115:563-571

مصطلحات موضوعية: Embryology, Health, Toxicology and Mutagenesis, Pediatrics, Perinatology and Child Health, Toxicology, Developmental Biology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::84f19d14641e3328bdbd1a048329f155
https://doi.org/10.1002/bdr2.2141

المؤلفون: Mathilde Pacault, Camille Verebi, Maureen Lopez, Nicolas Vaucouleur, Lucie Orhant, Nathalie Deburgrave, France Leturcq, Dominique Vidaud, Emmanuelle Girodon, Thierry Bienvenu, Juliette Nectoux

المصدر: Obstetrical & Gynecological Survey. 78:204-206

مصطلحات موضوعية: Obstetrics and Gynecology, General Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::3f97980aa8b42281c75b0acb609c0b4e
https://doi.org/10.1097/01.ogx.0000931668.13238.16

المؤلفون: Laurence Pacot, Valerie Pelletier, Albain Chansavang, Audrey Briand-Suleau, Cyril Burin des Roziers, Audrey Coustier, Theodora Maillard, Nicolas Vaucouleur, Lucie Orhant, Cécile Barbance, Alban Lermine, Nadim Hamzaoui, Djihad Hadjadj, Ingrid Laurendeau, Laïla El Khattabi, Juliette Nectoux, Michel Vidaud, Béatrice Parfait, Hélène Dollfus, Eric Pasmant, Dominique Vidaud

المصدر: Human Genetics. 142:1-9

مصطلحات موضوعية: Genetics, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::cc0cf96dd8d3f9c0d79038ea9fde42dd
https://doi.org/10.1007/s00439-022-02476-3

المؤلفون: Nihel Khoudour, Florence Delestre, Fabienne Jabot–Hanin, Anne Jouinot, Juliette Nectoux, Franck Letouneur, Brigitte Izac, Michel Vidal, Loïc Guillevin, Xavier Puéchal, Pierre Charles, Benjamin Terrier, Benoit Blanchet

المصدر: Arthritis & Rheumatology.

مصطلحات موضوعية: Rheumatology, Immunology, Immunology and Allergy

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0fcd43af871f9c2fb4f5d1cd05bec460
https://doi.org/10.1002/art.42556

المؤلفون: Thomas Huby, Edouard Le Guillou, Cyril Burin des Roziers, Laurence Pacot, Audrey Briand-Suleau, Albain Chansavang, Aurélie Toussaint, Véronique Duchossoy, Nicolas Vaucouleur, Virginie Benoit, Laurence Lodé, Clémence Molac, Marie-Odile North, Sarah Grotto, Vassilis Tsatsaris, Anne Jouinot, Béatrix Cochand-Priollet, Anne-Cécile Paepegaey, Juliette Nectoux, Lionel Groussin, Eric Pasmant

المصدر: The Journal of Clinical Endocrinology & Metabolism. 107:e1367-e1373

مصطلحات موضوعية: Adult, Male, endocrine system diseases, Hyperparathyroidism, Noninvasive Prenatal Testing, Endocrinology, Diabetes and Metabolism, Biochemistry (medical), Clinical Biochemistry, Biochemistry, Endocrinology, Pregnancy, Multiple Endocrine Neoplasia Type 1, Paternal Inheritance, Humans, Female, Genetic Testing

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09899c1e5c14d5ce5eb7f3e051b5e4c3
https://doi.org/10.1210/clinem/dgab894

المؤلفون: Camille Verebi, Juliette Nectoux, Philip Gorwood, Yann Le Strat, Philibert Duriez, Nicolas Ramoz, Thierry Bienvenu

المصدر: Progress in Neuro-Psychopharmacology and Biological Psychiatry. 125:110770

مصطلحات موضوعية: Pharmacology, Biological Psychiatry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::711dff2b54ae53d6b964530660a045c7
https://doi.org/10.1016/j.pnpbp.2023.110770

المؤلفون: Cardone, Nastasia, Taglietti, Valentina, Baratto, Serena, Kefi, Kaouthar, Periou, Baptiste, Gitiaux, Ciryl, Barnerias, Christine, Lafuste, Peggy, Pharm, France Leturcq, Pharm, Juliette Nectoux, Panicucci, Chiara, Desguerre, Isabelle, Bruno, Claudio, Authier, François-Jerome, Fiorillo, Chiara, Relaix, Frederic, Malfatti, Edoardo

المصدر: Acta Neuropathologica Communications; 8/21/2023, Vol. 11 Issue 1, p1-11, 11p

المؤلفون: Aurélien Perrin, Charles Van Goethem, Corinne Thèze, Jacques Puechberty, Thomas Guignard, Bérénice Lecardonnel, Delphine Lacourt, Corinne Métay, Arnaud Isapof, Sandra Whalen, Ana Ferreiro, Marie-Christine Arne-Bes, Susana Quijano-Roy, Juliette Nectoux, France Leturcq, Pascale Richard, Marion Larrieux, Anne Bergougnoux, Franck Pellestor, Michel Koenig, Mireille Cossée

المساهمون: MORNET, Dominique, Physiologie & médecine expérimentale du Cœur et des Muscles [U 1046] (PhyMedExp), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Montpellier (UM), Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Hôpital Arnaud de Villeneuve [CHRU Montpellier], Unité de Génétique Chromosomique [Montpellier], Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée [Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Hôpital Arnaud de Villeneuve [CHRU Montpellier], Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier)-Centre Hospitalier Régional Universitaire [Montpellier] (CHRU Montpellier), Université de Montpellier (UM), Centre de recherche en Myologie – U974 SU-INSERM, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU), CHU Pitié-Salpêtrière [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), CHU Trousseau [APHP], Unité de Biologie Fonctionnelle et Adaptative (BFA (UMR_8251 / U1133)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Centre Hospitalier Universitaire de Purpan (CHU Purpan), Handicap neuromusculaire : Physiopathologie, Biothérapie et Pharmacologies appliquées (END-ICAP), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ)-Institut National de la Santé et de la Recherche Médicale (INSERM), Hôpital Raymond Poincaré [AP-HP], Université Paris-Saclay, Université de Versailles Saint-Quentin-en-Yvelines - UFR Sciences de la santé Simone Veil (UVSQ Santé), Université de Versailles Saint-Quentin-en-Yvelines (UVSQ), Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Supported by AFM 21384 grant [The French Muscular Dystrophy Association (AFM-Téléthon)] (A.P.), the Délégation à la Recherche Clinique et à l’Innovation du Groupement de Coopération Sanitaire de la Mission d’Enseignement, de Recherche, de Référence et d’Innovation de Montpellier-Nîmes (A.P.), and the research platform Chromostem., C.T. and J.P. contributed equally to this work. F.P. and M.K. contributed equally to this work.

المصدر: Journal of Molecular Diagnostics
Journal of Molecular Diagnostics, In press, ⟨10.1016/j.jmoldx.2022.04.006⟩

مصطلحات موضوعية: MESH: Alternative Splicing, MESH: genetics Connectin, Exons, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, MESH: genetics, Pathology and Forensic Medicine, MESH: genetics Exons, MESH: genetics Humans Muscular Diseases, Alternative Splicing, MESH: genetics Protein Isoforms, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, Muscular Diseases, Molecular Medicine, Humans, Protein Isoforms, Connectin

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a614ceeba6edc978d60faafd7bde4be
https://pubmed.ncbi.nlm.nih.gov/35580751

المؤلفون: Mathilde Pacault, Camille Verebi, Maureen Lopez, Nicolas Vaucouleur, Lucie Orhant, Nathalie Deburgrave, France Leturcq, Dominique Vidaud, Emmanuelle Girodon, Thierry Bienvenu, Juliette Nectoux

المصدر: BJOG : an international journal of obstetrics and gynaecologyREFERENCES. 129(11)

مصطلحات موضوعية: Male, Pregnancy, Noninvasive Prenatal Testing, Prenatal Diagnosis, Mutation, Paternal Inheritance, Obstetrics and Gynecology, Humans, Female, Aneuploidy, Child, Cell-Free Nucleic Acids, Polymerase Chain Reaction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62dc46f2ffd5e5a579b07ea390530509
https://pubmed.ncbi.nlm.nih.gov/35486001

المؤلفون: Nicolas, Lebrun, Chloé, Delépine, Mohamed, Selloum, Hamid, Meziane, Juliette, Nectoux, Yann, Herault, Thierry, Bienvenu

المصدر: Brain research. 1772

مصطلحات موضوعية: Male, Mice, Knockout, Indoles, Behavior, Animal, Methyl-CpG-Binding Protein 2, Histone Deacetylase 6, Hydroxamic Acids, Microtubules, Histone Deacetylase Inhibitors, Mice, Inbred C57BL, Mice, Astrocytes, Exploratory Behavior, Rett Syndrome, Animals, Female, Social Behavior, Psychomotor Performance

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::e38046e875982c91266729b6b7254b23
https://pubmed.ncbi.nlm.nih.gov/34582789

المؤلفون: Juliette Nectoux, Isabelle Nelson, Hunter Best, Anne-Sophie Lia, Cécile Masson, Lucie Guyant-Maréchal, Jean Michel Pedespan, Karima Ghorab, Marie Anne Barthez, Youna Ha, Jean-François Deleuze, Rong Mao, Cécile Laroche-Raynaud, Kathryn J. Swoboda, Xavier Hernandorena, Yue Si, Annick Toutain, Louis Viollet

المساهمون: University of Utah School of Medicine [Salt Lake City], Hôpital Bretonneau, Centre Hospitalier Régional Universitaire de Tours (CHRU Tours), Hôpital Charles Nicolle [Rouen], CHU Limoges, Hôpital Dupuytren [CHU Limoges], Hôpital Pellegrin, CHU Bordeaux [Bordeaux]-Groupe hospitalier Pellegrin, Le CHCB, Centre Hospitalier de la Côte Basque, Commissariat à l'énergie atomique et aux énergies alternatives (CEA), Centre National de Génotypage (CNG), Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP), CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Institut de Myologie, Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Association française contre les myopathies (AFM-Téléthon)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS), Service de biochimie et de génétique moléculaire [CHU Cochin], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Cochin [AP-HP], Centre National de la Recherche Scientifique (CNRS)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Association française contre les myopathies (AFM-Téléthon)-Sorbonne Université (SU), CHU Rouen, Normandie Université (NU)-Normandie Université (NU), Centre Hospitalier de la Côte Basque (CHCB), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Centre de recherche en Myologie – U974 SU-INSERM, Institut National de la Santé et de la Recherche Médicale (INSERM)-Sorbonne Université (SU)

المصدر: European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2020, 63 (12), pp.104063. ⟨10.1016/j.ejmg.2020.104063⟩
European Journal of Medical Genetics, 2020, 63 (12), pp.104063. ⟨10.1016/j.ejmg.2020.104063⟩

مصطلحات موضوعية: Adult, Cytoplasmic Dyneins, Male, 0301 basic medicine, Heterozygote, Adolescent, [SDV]Life Sciences [q-bio], Mutation, Missense, 030105 genetics & heredity, Biology, Hyperreflexia, Lower motor neuron, Muscular Atrophy, Spinal, Upper Extremity, 03 medical and health sciences, Spinal muscular atrophies, Next generation sequencing, Reflex, Genetics, medicine, Humans, Exome, Child, Muscle, Skeletal, Genetics (clinical), Motor Neurons, Upper motor neuron, DYNC1H1, General Medicine, Spinal muscular atrophy, Middle Aged, medicine.disease, Penetrance, Pedigree, 3. Good health, Phenotype, 030104 developmental biology, medicine.anatomical_structure, Upper motor neuron syndrome, Lower Extremity, Child, Preschool, Chromosomal region, Female, medicine.symptom

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e224ac54b05249f7407c0588a4d241b
https://hal.sorbonne-universite.fr/hal-03182670

المؤلفون: Thierry Bienvenu, Franck Letourneur, Emmanuelle Olivier, Benjamin Saintpierre, Brigitte Izac, Marine Brousseau, Nicolas Cagnard, Juliette Nectoux, Nicolas Lebrun

المساهمون: Service de biochimie et de génétique moléculaire [CHU Cochin], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Hôpital Cochin [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), U 1016/ UMR 8104 Institut Cochin, Plate-Forme Séquençage et Génomique (Genom'IC), Institut National de la Santé et de la Recherche Médicale (INSERM), Institut de psychiatrie et neurosciences de Paris (IPNP - U1266 Inserm), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Paris (UP), Plateforme de Bioinformatique [Paris] (Fondation Imagine), Martinez Rico, Clara, Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité)

المصدر: Biochimica et Biophysica Acta-Molecular Basis of Disease
Biochimica et Biophysica Acta-Molecular Basis of Disease, Elsevier, 2020, 1866 (6), pp.165730. ⟨10.1016/j.bbadis.2020.165730⟩

مصطلحات موضوعية: 0301 basic medicine, congenital, hereditary, and neonatal diseases and abnormalities, Methyl-CpG-Binding Protein 2, [SDV]Life Sciences [q-bio], Mutant, Rett syndrome, Biology, Allelic Imbalance, MECP2, 03 medical and health sciences, 0302 clinical medicine, Genes, X-Linked, Gene expression, mental disorders, medicine, [SDV.BBM] Life Sciences [q-bio]/Biochemistry, Molecular Biology, Humans, [SDV.BBM]Life Sciences [q-bio]/Biochemistry, Molecular Biology, Allele, Molecular Biology, Gene, Alleles, Genetics, [SDV.MHEP] Life Sciences [q-bio]/Human health and pathology, medicine.disease, nervous system diseases, [SDV] Life Sciences [q-bio], 030104 developmental biology, Phenotype, Gene Expression Regulation, Mono-allelic expression, Mutation, Molecular Medicine, Human genome, Genomic imprinting, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24553fa3f68981fd56a725eb0f8218be
https://www.hal.inserm.fr/inserm-02571291/document

المؤلفون: N. Butoianu, Teresa Gidaro, E. Gargaun, Svetlana Gataullina, Ruxandra Cardas, Laurent Servais, Thierry Bienvenu, Dana Craiu, Juliette Nectoux, Catrinel Iliescu, Andreea Mihaela Seferian

مصطلحات موضوعية: musculoskeletal diseases, Central Nervous System, Male, Pediatrics, medicine.medical_specialty, Duchenne muscular dystrophy, Dystrophin, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Seizures, 030225 pediatrics, medicine, Humans, Protein Isoforms, Muscular dystrophy, Genetics (clinical), biology, Seizure types, business.industry, Infant, West Syndrome, medicine.disease, Hypsarrhythmia, Muscular Dystrophy, Duchenne, Epileptic spasms, Neurology, Child, Preschool, Pediatrics, Perinatology and Child Health, Mutation, biology.protein, Neurology (clinical), medicine.symptom, business, Spasms, Infantile, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c812d64fe4213f16663b6f04c5b9829
https://ora.ox.ac.uk/objects/uuid:07688860-7eed-4afd-90b9-2625c3ad5267

المؤلفون: Aurélia Gruber, Mathilde Pacault, Laila Allach El Khattabi, Nicolas Vaucouleur, Lucie Orhant, Thierry Bienvenu, Emmanuelle Girodon, Dominique Vidaud, France Leturcq, Catherine Costa, Franck Letourneur, Olivia Anselem, Vassilis Tsatsaris, François Goffinet, Géraldine Viot, Michel Vidaud, Juliette Nectoux

المصدر: Clinical Chemistry and Laboratory Medicine (CCLM). 56:728-738

مصطلحات موضوعية: Male, 0301 basic medicine, medicine.medical_specialty, Neurofibromatosis 1, Genotype, Clinical Biochemistry, Cystic Fibrosis Transmembrane Conductance Regulator, Prenatal diagnosis, medicine.disease_cause, Compound heterozygosity, Polymerase Chain Reaction, 03 medical and health sciences, 0302 clinical medicine, Prenatal Diagnosis, Molecular genetics, Humans, Medicine, Digital polymerase chain reaction, Genetics, Mutation, Fetus, 030219 obstetrics & reproductive medicine, business.industry, Biochemistry (medical), General Medicine, 030104 developmental biology, Neurodevelopmental Disorders, Female, Personalized medicine, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c58b17f732f6fdb21648b37327da9197
https://doi.org/10.1515/cclm-2017-0689

المؤلفون: Juliette Nectoux

المصدر: Molecular Diagnosis & Therapy. 22:139-148

مصطلحات موضوعية: 0301 basic medicine, Pharmacology, Massive parallel sequencing, business.industry, Non invasive, Medical laboratory, Prenatal diagnosis, General Medicine, Computational biology, 030204 cardiovascular system & hematology, Polymerase Chain Reaction, Human genetics, Fetal Diseases, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Prenatal Diagnosis, Genetics, Humans, Molecular Medicine, Medicine, Digital polymerase chain reaction, business, Genotyping

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::400c3de23272d6139c78acb8914e4e2d
https://doi.org/10.1007/s40291-017-0312-x