المؤلفون: Fabio, Rosa Angela, Gangemi, Antonio, Capri, Tindara, Budden, Sarojini, Falzone, Alessandra

المصدر: In Research in Developmental Disabilities May 2018 76:76-87

المؤلفون: Fabio, Rosa Angela, Giannatiempo, Samantha, Antonietti, Alessandro, Budden, Sarojini

المصدر: In Research in Developmental Disabilities 2009 30(1):136-145

المؤلفون: Matagne, Valerie, Wondolowski, Joyce, Frerking, Matthew, Shahidullah, Mohammad, Delamere, Nicholas A., Sandau, Ursula S., Budden, Sarojini, Ojeda, Sergio R.

المساهمون: 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), Gall, Valérie, Institut National de la Santé et de la Recherche Médicale (INSERM)-Aix Marseille Université (AMU)

المصدر: Brain Research
Brain Research, 2018, 1697, pp.45-52
Brain Research, Elsevier, 2018, 1697, pp.45-52

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Mecp2 deficiency, Neuronal morphology, Rett syndrome, Sodium-potassium ATPase, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, mental disorders, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics, nervous system diseases, Potassium efflux

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4f9dd12b743a8677e2b06311c19487c5
https://hal-amu.archives-ouvertes.fr/hal-01991342

المؤلفون: Budden, Sarojini S.

المصدر: American Annals of the Deaf. Aug 74 119(4):387-395.

Peer Reviewed: Y

Page Count: 9

Descriptors: Etiology, Exceptional Child Research, Foreign Countries, Genetics, Hearing Impairments, Incidence, Infants, Perinatal Influences, Prenatal Influences, Preschool Children, Statistical Data

مصطلحات جغرافية: Canada

المؤلفون: Budden, Sarojini S., Robinson, Geoffrey C., MacLean, C. Dunella, Cambon, Kenneth G.

المصدر: American Annals of the Deaf, 1974 Aug 01. 119(4), 387-395.

URL الوصول: https://www.jstor.org/stable/44387942

المؤلفون: Pereira Joseluiz, Angus John Clarke, Lars Edström, Naidu Sakkubai, Ingo Hansmann, Maria Anvret, Fengqing Xiang, Zhiping Zhang, Budden Sarojini, C. D. DeLozier-Blanchet

المصدر: Karolinska Institutet

مصطلحات موضوعية: Male, X Chromosome, Rett syndrome, Locus (genetics), Biology, Genetic determinism, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, Gene mapping, Rett Syndrome, Genetics, medicine, Humans, Skewed X-inactivation, Genetics (clinical), X chromosome, 0303 health sciences, 030305 genetics & heredity, Chromosome Mapping, Telomere, medicine.disease, Pedigree, Xq28, Female, 030217 neurology & neurosurgery, Microsatellite Repeats, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a55483ad51d523c69dd4d66cc499505b
https://doi.org/10.1136/jmg.35.4.297

المؤلفون: Stubbs, E. Gene, Budden, Sarojini S., Burger, Denis R., Vandenbark, Arthur A.

المصدر: Journal of Autism and Developmental Disorders. December 1980 10(4):451-458

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المؤلفون: Silva, Louisa M. T., Schalock, Mark, Gabrielsen, Kristen R., Budden, Sarojini S., Buenrostro, Martha, Horton, Gretchen

المصدر: Autism Research & Treatment; 3/24/2015, Vol. 2015, p1-16, 16p

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