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1دورية أكاديمية
المؤلفون: Kennedy, Joanna, Goudie, David, Blair, Edward, Chandler, Kate, Joss, Shelagh, McKay, Victoria, Green, Andrew, Armstrong, Ruth, Lees, Melissa, Kamien, Benjamin, Hopper, Bruce, Tan, Tiong Yang, Yap, Patrick, Stark, Zornitza, Okamoto, Nobuhiko, Miyake, Noriko, Matsumoto, Naomichi, Macnamara, Ellen, Murphy, Jennifer L, McCormick, Elizabeth, Hakonarson, Hakon, Falk, Marni J, Li, Dong, Blackburn, Patrick, Klee, Eric, Babovic-Vuksanovic, Dusica, Schelley, Susan, Hudgins, Louanne, Kant, Sarina, Isidor, Bertrand, Cogne, Benjamin, Bradbury, Kimberley, Williams, Mark, Patel, Chirag, Heussler, Helen, Duff-Farrier, Celia, Lakeman, Phillis, Scurr, Ingrid, Kini, Usha, Elting, Mariet, Reijnders, Margot, Schuurs-Hoeijmakers, Janneke, Wafik, Mohamed, Blomhoff, Anne, Ruivenkamp, Claudia AL, Nibbeling, Esther, Dingemans, Alexander JM, Douine, Emilie D, Nelson, Stanley F, Hempel, Maja, Bierhals, Tatjana, Lessel, Davor, Johannsen, Jessika, Arboleda, Valerie A, Newbury-Ecob, Ruth
المصدر: Genetics in Medicine. 21(4)
مصطلحات موضوعية: Biological Sciences, Genetics, Prevention, Brain Disorders, Rare Diseases, Pediatric, Clinical Research, Digestive Diseases, Intellectual and Developmental Disabilities (IDD), Aetiology, 2.1 Biological and endogenous factors, Adolescent, Adult, Child, Child, Preschool, Chromosome Deletion, Developmental Disabilities, Exome, Female, Genetic Association Studies, Genotype, Histone Acetyltransferases, Humans, Infant, Intellectual Disability, Male, Microcephaly, Mutation, Phenotype, Protein Isoforms, Young Adult, genetic diagnosis, phenotypic spectrum, KAT6A syndrome, chromatin modifiers, intellectual disability, DDD Study, KAT6A syndrome, chromatin modifiers, intellectual disability, Clinical Sciences, Genetics & Heredity
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/79s761gbTest
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2دورية أكاديمية
المؤلفون: French, Courtney E, Dolling, Helen, Mégy, Karyn, Sanchis-Juan, Alba, Kumar, Ajay, Delon, Isabelle, Wakeling, Matthew, Mallin, Lucy, Agrawal, Shruti, Austin, Topun, Walston, Florence, Park, Soo-Mi, Parker, Alasdair, Piyasena, Chinthika, Bradbury, Kimberley, Next Generation Children’s Project Consortium, Ellard, Sian, Rowitch, David H, Raymond, F Lucy
المصدر: essn: 2666-2477 ; nlmid: 101772885
مصطلحات موضوعية: genomics, mendelian disorders, paediatrics, rapid diagnostic whole genome, rare disease
وصف الملف: application/pdf
الإتاحة: https://doi.org/10.17863/CAM.85644Test
https://www.repository.cam.ac.uk/handle/1810/338232Test -
3دورية أكاديمية
المؤلفون: French, Courtney E., Dolling, Helen, Mégy, Karyn, Sanchis-Juan, Alba, Kumar, Ajay, Delon, Isabelle, Wakeling, Matthew, Mallin, Lucy, Agrawal, Shruti, Austin, Topun, Walston, Florence, Park, Soo-Mi, Parker, Alasdair, Piyasena, Chinthika, Bradbury, Kimberley, Ellard, Sian, Rowitch, David H., Raymond, F. Lucy
المساهمون: Isaac Newton Trust, NIHR Cambridge Biomedical Research Centre, Rosetrees Trust, NIHR BioResource
المصدر: Human Genetics and Genomics Advances ; volume 3, issue 3, page 100113 ; ISSN 2666-2477
مصطلحات موضوعية: Genetics (clinical), Molecular Medicine
الإتاحة: https://doi.org/10.1016/j.xhgg.2022.100113Test
https://api.elsevier.com/content/article/PII:S266624772200029X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S266624772200029X?httpAccept=text/plainTest -
4دورية أكاديمية
المؤلفون: Kennedy, Joanna, Goudie, David, Blair, Edward, Chandler, Kate, Joss, Shelagh, McKay, Victoria, Green, Andrew, Armstrong, Ruth, Lees, Melissa, Kamien, Benjamin, Hopper, Bruce, Tan, Tiong Yang, Yap, Patrick, Stark, Zornitza, Okamoto, Nobuhiko, Miyake, Noriko, Matsumoto, Naomichi, Macnamara, Ellen, Murphy, Jennifer L., McCormick, Elizabeth, Hakonarson, Hakon, Falk, Marni J., Li, Dong, Blackburn, Patrick, Klee, Eric, Babovic-Vuksanovic, Dusica, Schelley, Susan, Hudgins, Louanne, Kant, Sarina, Isidor, Bertrand, Cogne, Benjamin, Bradbury, Kimberley, Williams, Mark, Patel, Chirag, Heussler, Helen, Duff-Farrier, Celia, Lakeman, Phillis, Scurr, Ingrid, Kini, Usha, Elting, Mariet, Reijnders, Margot, Schuurs-Hoeijmakers, Janneke, Wafik, Mohamed, Blomhoff, Anne, Ruivenkamp, Claudia A. L., Nibbeling, Esther, Dingemans, Alexander J. M., Douine, Emilie D., Nelson, Stanley F., Hempel, Maja, Bierhals, Tatjana, Lessel, Davor, Johannsen, Jessika, Arboleda, Valerie A., Newbury-Ecob, Ruth
المصدر: Kennedy , J , Goudie , D , Blair , E , Chandler , K , Joss , S , McKay , V , Green , A , Armstrong , R , Lees , M , Kamien , B , Hopper , B , Tan , T Y , Yap , P , Stark , Z , Okamoto , N , Miyake , N , Matsumoto , N , Macnamara , E , Murphy , J L , McCormick , E , Hakonarson , H , Falk , M J , Li , D , Blackburn , P , ....
الإتاحة: https://doi.org/10.1038/s41436-020-00944-7Test
https://doi.org/10.1038/s41436-018-0259-2Test
https://research.vumc.nl/en/publications/fa0da8e1-b08a-4d21-abfd-0966d2941410Test
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85089491461&origin=inwardTest
https://www.ncbi.nlm.nih.gov/pubmed/32814847Test -
5دورية أكاديمية
المؤلفون: Pagnamenta, Alistair T., Kaisaki, Pamela J., Bennett, Fenella, Burkitt‐Wright, Emma, Martin, Hilary C., Ferla, Matteo P., Taylor, John M., Gompertz, Lianne, Lahiri, Nayana, Tatton‐Brown, Katrina, Newbury‐Ecob, Ruth, Henderson, Alex, Joss, Shelagh, Weber, Astrid, Carmichael, Jenny, Turnpenny, Peter D., McKee, Shane, Forzano, Francesca, Ashraf, Tazeen, Bradbury, Kimberley, Shears, Deborah, Kini, Usha, de Burca, Anna, Blair, Edward, Taylor, Jenny C., Stewart, Helen
المساهمون: National Institute for Health Research, Wellcome Trust
المصدر: Clinical Genetics ; volume 95, issue 6, page 693-703 ; ISSN 0009-9163 1399-0004
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6دورية أكاديمية
المؤلفون: Kennedy, Joanna, Goudie, David, Blair, Edward, Chandler, Kate, Joss, Shelagh, McKay, Victoria, Green, Andrew, Armstrong, Ruth, Lees, Melissa, Kamien, Benjamin, Hopper, Bruce, Tan, Tiong Yang, Yap, Patrick, Stark, Zornitza, Okamoto, Nobuhiko, Miyake, Noriko, Matsumoto, Naomichi, Macnamara, Ellen, Murphy, Jennifer L, McCormick, Elizabeth, Hakonarson, Hakon, Falk, Marni J, Li, Dong, Blackburn, Patrick, Klee, Eric, Babovic-Vuksanovic, Dusica, Schelley, Susan, Hudgins, Louanne, Kant, Sarina, Isidor, Bertrand, Cogne, Benjamin, Bradbury, Kimberley, Williams, Mark, Patel, Chirag, Heussler, Helen, Duff-Farrier, Celia, Lakeman, Phillis, Scurr, Ingrid, Kini, Usha, Elting, Mariet, Reijnders, Margot, Schuurs-Hoeijmakers, Janneke, Wafik, Mohamed, Blomhoff, Anne, Ruivenkamp, Claudia A. L., Nibbeling, Esther, Dingemans, Alexander J. M., Douine, Emilie D., Nelson, Stanley F., Arboleda, Valerie A., Newbury-Ecob, Ruth
المصدر: Deciphering Developmental Disorders (DDD) Study , Kennedy , J , Goudie , D , Blair , E , Chandler , K , Joss , S , McKay , V , Green , A , Armstrong , R , Lees , M , Kamien , B , Hopper , B , Tan , T Y , Yap , P , Stark , Z , Okamoto , N , Miyake , N , Matsumoto , N , Macnamara , E , Murphy , J L , McCormick , E , Hakonarson , H , Falk , M J , Li , ....
مصطلحات موضوعية: KAT6A syndrome, chromatin modifiers, intellectual disability, genetic diagnosis, phenotypic spectrum, /dk/atira/pure/subjectarea/asjc/2700/2716, name=Genetics(clinical)
الإتاحة: https://doi.org/10.1038/s41436-018-0259-2Test
https://discovery.dundee.ac.uk/en/publications/d3084c02-f3c8-4c36-85d4-05c9a4530cacTest
http://www.scopus.com/inward/record.url?scp=85053824960&partnerID=8YFLogxKTest -
7دورية أكاديمية
المؤلفون: Griffin, Lewis D., Sutcliffe, Alastair G., Bradbury, Kimberley, Kumble, Smitha, Mylonas, Dimitris, Baker, Alastair
المصدر: Color Research & Application ; volume 40, issue 6, page 585-591 ; ISSN 0361-2317 1520-6378
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8دورية أكاديمية
المؤلفون: Bradbury, Kimberley, Sutcliffe, Alastair
المصدر: Paediatrics and Child Health ; volume 24, issue 4, page 172-176 ; ISSN 1751-7222
مصطلحات موضوعية: Pediatrics, Perinatology and Child Health
الإتاحة: https://doi.org/10.1016/j.paed.2013.09.004Test
https://api.elsevier.com/content/article/PII:S175172221300228X?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S175172221300228X?httpAccept=text/plainTest -
9دورية أكاديمية
المؤلفون: Griffin, Lewis D., Sutcliffe, Alastair G., Bradbury, Kimberley, Kumble, Smitha, Mylonas, Dimitris, Baker, Alastair
المصدر: Color Research & Application; Dec2015, Vol. 40 Issue 6, p585-591, 7p
مصطلحات موضوعية: SPECTRAL reflectance, FECES