المؤلفون: Daniel E. McGinn, T. Blaine Crowley, Tracy Heung, Oanh Tran, Edward Moss, Elaine H. Zackai, Beverly S. Emanuel, Eva W. C. Chow, Bernice E. Morrow, Ann Swillen, Anne S. Bassett, Donna M. McDonald-McGinn

المصدر: Genes; Volume 13; Issue 10; Pages: 1800

مصطلحات موضوعية: Genetics & Heredity, intellect, de novo, Science & Technology, familial, CHILDREN, 22q, FSIQ, Chromosomes, chromosome, deletion, DiGeorge, parent-of-origin, Intellectual Disability, PSYCHOSOCIAL ADJUSTMENT, DiGeorge Syndrome, Genetics, Humans, Chromosome Deletion, Life Sciences & Biomedicine, Genetics (clinical)

وصف الملف: Electronic; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6468bab070fc9796f70a3930443f19d3Test
https://lirias.kuleuven.be/handle/20.500.12942/706653Test

المؤلفون: Ming Xiao, Lahari Uppuluri, Beverly S. Emanuel, Donna M. McDonald-McGinn, Daniel E. McGinn, Deanne Taylor, Benjamin A. Silva, T. Blaine Crowley, Michael Xie, Heba Z. Abid, Bernice E. Morrow, Steven Pastor, Elaine H. Zackai, Oanh Tran, Alice Bailey, Eleanor Young, Danielle Carrado, Andrea Jin

المصدر: Scientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
Scientific Reports

مصطلحات موضوعية: Male, 0301 basic medicine, Chromosomes, Human, Pair 22, Non-allelic homologous recombination, lcsh:Medicine, Biology, Genome informatics, Article, 03 medical and health sciences, Segmental Duplications, Genomic, 0302 clinical medicine, DiGeorge Syndrome, Humans, Homologous Recombination, lcsh:Science, Gene, Alleles, Segmental duplication, Genome, Multidisciplinary, Genome, Human, Haplotype, Breakpoint, lcsh:R, Chromosome Mapping, Low copy repeats, 030104 developmental biology, Haplotypes, Evolutionary biology, 030220 oncology & carcinogenesis, Female, Human genome, lcsh:Q, Chromosome Deletion, Homologous recombination

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32c1b75f551f3d9ba05ded3008e83778Test
http://link.springer.com/article/10.1038/s41598-020-69134-4Test

المؤلفون: Lisanne Vervoort, Tamim H. Shaikh, Beverly S. Emanuel, Elfi Vergaelen, Ming Xiao, Steven Pastor, Wolfram Demaerel, Donna M. McDonald-McGinn, Matthew S. Hestand, Ann Swillen, Yulia Mostovoy, Elizabeth A. Geiger, Pui-Yan Kwok, Joris Vermeesch, Bernice E. Morrow, Curtis R. Coughlin, Stephen K. Chow, Feyza Yilmaz

المصدر: Genome research, vol 29, iss 9

مصطلحات موضوعية: Primates, Genome instability, 22q11 Deletion Syndrome, Evolution, Bioinformatics, Chromosomes, Human, Pair 22, Non-allelic homologous recombination, Biology, Medical and Health Sciences, Genome, Chromosomes, Fluorescence, Repetitive Sequences, Cell Line, Evolution, Molecular, 03 medical and health sciences, 0302 clinical medicine, Chromosomal Instability, Chromosome instability, Genetics, Animals, Humans, 2.1 Biological and endogenous factors, Aetiology, Allele, In Situ Hybridization, Fluorescence, In Situ Hybridization, Genetics (clinical), Repetitive Sequences, Nucleic Acid, 030304 developmental biology, 0303 health sciences, Nucleic Acid, Research, Human Genome, Chromosome Mapping, Molecular, Low copy repeats, Biological Sciences, Evolutionary biology, Pair 22, Chromosome 22, 030217 neurology & neurosurgery, Human

وصف الملف: Print; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce69d30c7c07cbca901d9297cc285853Test
https://doi.org/10.1101/gr.248682.119Test

المؤلفون: Elizabeth Goldmuntz, Beverly S. Emanuel, Omobola O. Oluwafemi, Fadi I Musfee, A. J. Agopian, Hongbo Xie, Tingwei Guo, Hakon Hakonarson, Laura E. Mitchell, Deanne Taylor, Donna M McDonald-McGinn, Bernice E. Morrow

المصدر: Genes
Volume 12
Issue 7
Genes, Vol 12, Iss 1030, p 1030 (2021)

مصطلحات موضوعية: 0301 basic medicine, Heart Defects, Congenital, Genotype, Genome-wide association study, Single-nucleotide polymorphism, QH426-470, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, Article, Conotruncal heart defects, 03 medical and health sciences, 0302 clinical medicine, Conotruncal defect, Genetics, DiGeorge Syndrome, Humans, Deletion syndrome, Genetic Testing, Gene, Genetics (clinical), genome-wide association study, congenital, United States, 030104 developmental biology, Great vessels, Multiple comparisons problem, heart defects, Chromosome Deletion

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::342116ad277cb066b5534b9439023734Test
http://europepmc.org/articles/PMC8306129Test

المؤلفون: Deanne Taylor, Mark Yandell, Hakon Hakonarson, Elizabeth Goldmuntz, Fadi I Musfee, Martin Tristani-Firouzi, Bernice E. Morrow, W. Scott Watkins, Laura E. Mitchell, A. J. Agopian

المصدر: Genes
Volume 12
Issue 5
Genes, Vol 12, Iss 655, p 655 (2021)

مصطلحات موضوعية: 0301 basic medicine, Heart Defects, Congenital, Genotype, heart, QH426-470, 030204 cardiovascular system & hematology, Biology, Polymorphism, Single Nucleotide, Article, Conotruncal heart defects, genome-wide, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Risk Factors, Ventricular outflow tract, Humans, genetics, Cytoskeleton, gene, Gene, Exome, Genetics (clinical), Genetics, Genome, Human, Genetic variants, association, congenital, conotruncal, malformation, 030104 developmental biology, Bonferroni correction, Case-Control Studies, symbols, case-parent trios, case-control

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7995e5b10872c7d355952404cca4c33eTest
https://pubmed.ncbi.nlm.nih.gov/33925651Test

المؤلفون: Maude Schneider, Doron Gothelf, Marianne Bernadette van den Bree, Carrie E. Bearden, Donna M. McDonald-McGinn, Marco Armando, Raquel E. Gur, Jordi Rosell, Joris Vermeesch, Ann Swillen, Therese van Amelsvoort, Jacob A. S. Vorstman, Robert J. Shprintzen, Tao Wang, Clodagh M. Murphy, Kieran C. Murphy, Tingwei Guo, Terrence B. Crowley, Jasna Raventos, Nicole Philip, Sasja N. Duijff, Elaine H. Zackai, Maria Pontillo, Jeroen Breckpot, Stephan Eliez, Alexander Diacou, Beverly S. Emanuel, Stefano Vicari, Michael John Owen, Maria Niarchou, Claudia Ornstein, Jaume Morey‐Cañellas, Anne S. Bassett, Yingjie Zhao, Ania Fiksinski, Rens Evers, Elemi J. Breetvelt, Antonino Buzzanca, Sixto García-Miñaur, Bernice E. Morrow, Eva W.C. Chow, Wendy R. Kates, Linda E. Campbell, Damian Heine-Suñer

المساهمون: RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, MUMC+: MA Med Staf Spec Psychiatrie (9)

المصدر: American Journal of Medical Genetics. A, Vol. 176, No 10 (2018) pp. 2172-2181
American Journal of Medical Genetics Part A, 176(10), 2172-2181. Wiley
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
American journal of medical genetics. Part A, vol 176, iss 10

مصطلحات موضوعية: 0301 basic medicine, Male, Chromosomes, Human, Pair 22, Intellectual disability, DEVELOPMENTAL TRAJECTORIES, INTELLIGENCE, ddc:616.89, 0302 clinical medicine, Cognitive decline, BRAIN, Child, Genetics (clinical), Intelligence Tests, Pediatric, education.field_of_study, Intelligence quotient, CARDIO-FACIAL-SYNDROME, Low copy repeats, CONGENITAL HEART-DISEASE, low copy repeat, VELOCARDIOFACIAL SYNDROME, intellectual disability, Cohort, Female, SCHOOL-AGED CHILDREN, Chromosome Deletion, Haploinsufficiency, Deletion size, deletion size, Human, Adult, medicine.medical_specialty, Adolescent, Population, Clinical Sciences, Segmental duplication, Low copy repeat, segmental duplication, Biology, Article, Chromosomes, 03 medical and health sciences, NEURODEVELOPMENTAL OUTCOMES, Clinical Research, Internal medicine, medicine, DiGeorge Syndrome, Genetics, Acquired Cognitive Impairment, Humans, education, International 22q11.2 Brain and Behavior Consortium, medicine.disease, Brain Disorders, Institutional repository, 030104 developmental biology, Endocrinology, IQ, 22q11.2 deletion syndrome, COGNITIVE DECLINE, Pair 22, FOLLOW-UP, 030217 neurology & neurosurgery

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c08da23afa70859c4fc6d6aa3b110d39Test
https://doi.org/10.1002/ajmg.a.40359Test

المؤلفون: Richard Duncan, Tao Wang, Carrie E. Bearden, David J. Cutler, Stephen T. Warren, Maria Pontillo, Robert Sean Gallagher, Elemi J. Breetvelt, Tingwei Guo, Nancy J. Butcher, Jennifer G. Mulle, Claudia Ornstein, Claudia Vingerhoets, Clodagh M. Murphy, Ehud Mekori-Domachevsky, Wendy R. Kates, Jacob A. S. Vorstman, Tracy Heung, Joris Vermeesch, Maria Gudbrandsen, Ann Swillen, H. Richard Johnston, Oanh Tran, Marco Armando, Joseph F. Cubells, Raoul Belzeaux, Jeroen Breckpot, Bruno Marino, Tony J. Simon, Harold I. Salmons, Maria Jalbrzikowski, Wanda Fremont, Anna J. Voss, Worrawat Engchuan, Opal Y. Ousley, Stefano Vicari, Jordi Rosell, Sixto García-Miñaur, Declan G. Murphy, Alexander Diacou, Ania Fiksinski, Abraham Weizman, Edward Moss, Stephan Eliez, Miri Carmel, Vandana Shashi, Anne S. Bassett, Ronnie Weinberger, Hayley Moss, Marianne Bernadette van den Bree, Kelly Schoch, Maude Schneider, Linda E. Campbell, Sasja N. Duijff, Eileen Daly, Annick Vogels, Stephen R. Hooper, David Fraguas, Sarah E. Prasad, Chelsea Lowther, Michael John Owen, Frédérique Béna, Gabriela M. Repetto, Eva W.C. Chow, Bernice E. Morrow, Robert J. Sharkus, Celso Arango, Christian R. Marshall, Jasna Raventos-Simic, Jaume Morey-Canyelles, Tiffany Busa, Andrea Jin, James T.R. Walters, Leila Kushan, Wolfram Demaerel, Monica E. Calkins, Jhih Rong Lin, Elaine H. Zackai, Esther D.A. van Duin, Antonio Buzzanca, Corrado Sandini, Kieran C. Murphy, Beverly S. Emanuel, Erik Boot, Maria Niarchou, Nigel Williams, Elfi Vergaelen, Maria Cristina Digilio, Daniele Merico, Karlene Coleman, Gregory A. Costain, Matthew S. Hestand, Peter Holmans, Michael E. Zwick, Michael P. Epstein, Damià H. Suñer, Yingjie Zhao, Marta Unolt, Kathryn McCabe, Aaron M. Holleman, Zhengdong Zhang, Rosemarie Fritsch, Alex V. Kotlar, Elena Michaelovsky, T. Blaine Crowley, Brenna Lilley, Sunny X. Tang, Rens Evers, Ruben C. Gur, Isabelle Cleynen, Flora Tassone, Nicole Philip, Kevin M. Antshel, Koen Devriendt, Antonio F. Pardiñas, Pankaj Chopra, Thomas Monfeuga, Fabio Di Fabio, Therese van Amelsvoort, Aaron Golden, Doron Gothelf, Donna M. McDonald-McGinn, Raquel E. Gur, Daniel E. McGinn

المساهمون: Catholic University of Leuven - Katholieke Universiteit Leuven (KU Leuven), The Hospital for sick children [Toronto] (SickKids), Emory University [Atlanta, GA], Cardiff University, University of Pennsylvania [Philadelphia], Albert Einstein College of Medicine [New York], University Hospitals Leuven [Leuven], University of Toronto, University Medical Center [Utrecht], University of California, Children’s Hospital of Philadelphia (CHOP ), Emory University School of Medicine, University Health Network, Centre for Addiction and Mental Health [Toronto] (CAMH), Maastricht University [Maastricht], Universidad de Chile, Clínica Alemana & Universidad del Desarrollo, Royal College of Surgeons in Ireland (RCSI), King‘s College London, Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome], Children's Hospital Bambino Gesù [Rome, Italie], Tel Aviv University [Tel Aviv], The Edmond and Lily Safra Children's Hospital [Tel-Hahsomer, Israel], University of Pittsburgh School of Medicine, Pennsylvania Commonwealth System of Higher Education (PCSHE), University of Geneva [Switzerland], Geneva University Hospitals and Geneva University, Syracuse University, SUNY Upstate Medical University, State University of New York (SUNY), Hôpital Sainte-Marguerite [CHU - APHM] (Hôpitaux Sud ), Hôpital d'Enfants de la Timone [Marseille], Assistance Publique - Hôpitaux de Marseille (APHM), Marseille medical genetics - Centre de génétique médicale de Marseille (MMG), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM), University of Newcastle [Australia] (UoN), University of North Carolina [Chapel Hill] (UNC), University of North Carolina System (UNC), Duke University School of Medicine, University of California [Davis] (UC Davis), Universidad Complutense de Madrid = Complutense University of Madrid [Madrid] (UCM), La Paz University Hospital, Hospital Universitario Son Espases, University of Pennsylvania, University of California (UC), Universidad de Chile = University of Chile [Santiago] (UCHILE), Università degli Studi di Roma 'La Sapienza' = Sapienza University [Rome] (UNIROMA), Tel Aviv University (TAU), Université de Genève = University of Geneva (UNIGE), University of Newcastle [Callaghan, Australia] (UoN), Caugant, Julien, RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, MUMC+: MA Med Staf Spec Psychiatrie (9)

المصدر: Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group

مصطلحات موضوعية: 0301 basic medicine, [SDV]Life Sciences [q-bio], VARIANTS, Cohort Studies, 0302 clinical medicine, Medicine, Copy-number variation, BRAIN, ddc:616, Genetics, education.field_of_study, PSYCHIATRIC-DISORDERS, ASSOCIATION, 3. Good health, [SDV] Life Sciences [q-bio], Psychiatry and Mental health, Schizophrenia, Cohort, BEHAVIOR, Adult, DATABASE, Population, COPY-NUMBER VARIATION, Article, 03 medical and health sciences, Cellular and Molecular Neuroscience, Settore MED/39 - NEUROPSICHIATRIA INFANTILE, mental disorders, DiGeorge Syndrome, Humans, genetics, 22q11deletion syndrome, schizophrenia, education, Molecular Biology, Gene, Microarray analysis techniques, business.industry, MUTATIONS, CONSORTIUM, medicine.disease, Institutional repository, INDIVIDUALS, 030104 developmental biology, Psychotic Disorders, Case-Control Studies, 22q11.2 deletion syndrome, genetic factors, Polygenic risk score, business, 030217 neurology & neurosurgery, International 22q11.2DS Brain and Behavior Consortium

وصف الملف: application/pdf; Print-Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c91788310dcf6c66ef3ac3973170b9Test
http://hdl.handle.net/20.500.12278/33344Test

المؤلفون: Claudia Ornstein, Anne S. Bassett, Matthew S. Hestand, Bruno Marino, Kelly Schoch, Tony J. Simon, Therese van Amelsvoort, Doron Gothelf, Carrie E. Bearden, Elemi J. Breetvelt, Michael P. Epstein, Tiffany Busa, Robert J. Shprintzen, David Cutler, Tao Wang, Leila Kushan-Wells, Donna M. McDonald-McGinn, Raquel E. Gur, Hayley Moss, Esther D. A. van Duin, B Dallapiccola, Joris Vermeesch, Clodagh M. Murphy, Yingjie Zhao, Rens Evers, María Angeles de la Fuente Sanches, Ann Swillen, H. Richard Johnston, Maria Pontillo, Steve Warren, Guido Lattanzi, Michael E. Zwick, Jacob A. S. Vorstman, Jeroen Breckpot, Oanh Tran, Stylianos E. Antonarakis, Stefano Vicari, Andrea Jin, Alexander Diacou, Miri Carmel, Christian R. Marshall, Abraham Weizman, Bernice E. Morrow, Fadi I Musfee, Wendy R. Kates, Michael John Owen, Fabio Di Fabio, Marco Armando, Erik Boot, Claudia Vingerhoets, Elizabeth Goldmuntz, Massimo Biondi, Kieran C. Murphy, Nancy Butcher, Declan G. Murphy, Candice K. Silversides, Isabelle Cleynen, T. Blaine Crowley, Vandana Shashi, Linda E. Campbell, Elaine H. Zackai, Ronnie Weinberger, Sixto García-Miñaur, Marianne Bernadette van den Bree, Fernando García Algas, Damian Heine-Suñer, Tracy Heung, Daniel E. McGinn, Maude Schneider, Stephan Eliez, Marta Unolt, Stephen R. Hooper, Kathryn McCabe, A. J. Agopian, Tingwei Guo, Zhengdong Zhang, Rosemarie Fritsch, Luis Fernández, Beverly S. Emanuel, Elfi Vergaelen, Alejandra Laorden-Nieto, Flora Tassone, Gabriela M. Repetto, Laura E. Mitchell, Antonino Buzzanca, Elena Michaelovsky, M. Cristina Digilio, Nicole Philip

المساهمون: RS: MHeNs - R2 - Mental Health, Psychiatrie & Neuropsychologie, MUMC+: MA Med Staf Spec Psychiatrie (9), Antonarakis, Stylianos

المصدر: American Journal of Human Genetics, 106(1), 26-40. Cell Press
Am J Hum Genet
American Journal of Human Genetics, Vol. 106, No 1 (2020) pp. 26-40
American journal of human genetics, vol 106, iss 1

مصطلحات موضوعية: Male, Heart disease, PREDICTION, Chromosomes, Human, Pair 22, Haploinsufficiency, Cardiovascular, Medical and Health Sciences, Genetic modifier, Proto-Oncogene Mas, Linkage Disequilibrium, Cohort Studies, Congenital, ddc:616.89, Segmental Duplications, Genomic, DiGeorge syndrome, 2.1 Biological and endogenous factors, Chromosome 22q11.2 deletion syndrome, Copy-number variation, Aetiology, Genetics (clinical), Heart Defects, Pediatric, Genetics & Heredity, Genetics, cardio-facial syndrome, II DEFICIENCY, 0303 health sciences, variants, MOLECULAR DEFINITION, 030305 genetics & heredity, TBX1, Single Nucleotide, Biological Sciences, Segmental Duplications, Complex trait, Heart Disease, Phenotype, Female, tbx1 haploinsufficiency, Chromosome Deletion, Human, Heart Defects, Congenital, prevalence, Biology, Polymorphism, Single Nucleotide, Chromosomes, Article, 03 medical and health sciences, Complete sequence, Clinical Research, LOW-COPY REPEATS, medicine, Humans, Polymorphism, Allele, Conotruncal heart defects, International 22q11.2 Brain and Behavior Consortium, 030304 developmental biology, Sequence (medicine), Congenital heart disease, Copy number variation, Human Genome, association, CRKL, medicine.disease, chromosome 22q11.2 deletion syndrome, complex trait, congenital heart disease, conotruncal heart defects, copy number variation, genetic association, genetic modifier, haploinsufficiency, Case-Control Studies, Genome-Wide Association Study, Genomic, Genetic association, Pair 22

وصف الملف: application/pdf; Print-Electronic

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8700304c185800fa1b2e56de201d2874Test
https://cris.maastrichtuniversity.nl/en/publications/fcebc151-7a92-4dbe-8f36-bd15cb7462bbTest

المؤلفون: Bernice E. Morrow, Erica Hasten

المصدر: PLoS Genetics
PLoS Genetics, Vol 15, Iss 8, p e1008301 (2019)

مصطلحات موضوعية: Male, Cancer Research, Embryology, Parathyroid, Pharyngeal pouch, Mutant, QH426-470, Epithelium, Mice, 0302 clinical medicine, Animal Cells, Morphogenesis, Medicine and Health Sciences, Genetics (clinical), Zebrafish, 0303 health sciences, Endoderm, Eukaryota, Gene Expression Regulation, Developmental, Forkhead Transcription Factors, Heart, Animal Models, Thymus, medicine.anatomical_structure, Experimental Organism Systems, Osteichthyes, embryonic structures, Vertebrates, Female, Cellular Types, Anatomy, Research Article, TBX1, JAG1, Immunology, Endocrine System, Mice, Transgenic, Biology, Research and Analysis Methods, 03 medical and health sciences, Model Organisms, stomatognathic system, Pharyngeal apparatus, Ectoderm, medicine, Genetics, DiGeorge Syndrome, Animals, Humans, Molecular Biology, Ecology, Evolution, Behavior and Systematics, ALCAM, 030304 developmental biology, Myocardium, Embryos, Wild type, Organisms, Biology and Life Sciences, Epithelial Cells, Cell Biology, Morphogenic Segmentation, Embryo, Mammalian, Molecular biology, Disease Models, Animal, Biological Tissue, Fish, Branchial Region, Immune System, Mutation, Animal Studies, T-Box Domain Proteins, 030217 neurology & neurosurgery, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6986907bc0f2f082729d604e6c848ec1Test
http://europepmc.org/articles/PMC6709926Test

المؤلفون: Elizabeth Goldmuntz, Hakon Hakonarson, Bernice E. Morrow, Elaine H. Zackai, Hongbo Xie, Deanne Taylor, Dwight Stambolian, Beverly S. Emanuel, Donna M. McDonald-McGinn, Zhe Zhang

المصدر: Birth Defects Res

مصطلحات موضوعية: 0301 basic medicine, Adult, Heart Defects, Congenital, Male, Embryology, Microarray, DNA Copy Number Variations, Health, Toxicology and Mutagenesis, Gene regulatory network, 030105 genetics & heredity, Biology, Toxicology, Article, 03 medical and health sciences, Mice, Risk Factors, Gene expression, DiGeorge Syndrome, Animals, Humans, Gene Regulatory Networks, Copy-number variation, Gene, Genetics, Regulation of gene expression, Heart development, Infant, Newborn, Computational Biology, Gene Expression Regulation, Developmental, Embryo, Heart, Middle Aged, 030104 developmental biology, Gene Ontology, Pediatrics, Perinatology and Child Health, Female, Transcriptome, Developmental Biology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2ecc5372a623c1625cad45edbf8dce6Test
https://europepmc.org/articles/PMC7398559Test/