Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Me Suzanne Lewis"'
Autor:
Me Suzanne Lewis
Publikováno v:
Clinical Genetics. 58:12-15
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e15bcc0ccb163636bda795da58576f8f
https://doi.org/10.1034/j.1399-0004.2000.580102.x
https://doi.org/10.1034/j.1399-0004.2000.580102.x
Autor:
Cynthia J. Forster-Gibson, Antonio M. Persico, Evica Rajcan-Separovic, Chelsea Reesor, Xudong Liu, Melissa Hudson, Chansonette Harvard, Jeanette J. A. Holden, Alana Lee, Ira L. Cohen, Albert E. Chudley, Me Suzanne Lewis, Patrick Malenfant, Ying Qiao
Reports of unrelated individuals with autism spectrum disorder (ASD) and similar clinical features having overlapping de novo interstitial deletions at 2p15-p16.1 suggest that this region harbors a gene(s) important to the development of autism. We m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df0bff916e8542645e812d2dad88126f
https://hdl.handle.net/11380/1250970
https://hdl.handle.net/11380/1250970
Fetal gene therapy confers stable gene expression, germline and widespread somatic cell transfection
Autor:
Me Suzanne Lewis
Publikováno v:
Clinical Genetics. 55:82-84
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3e506c681e2e4b55cf1e51842bb93fa6
https://doi.org/10.1034/j.1399-0004.1999.550202-3.x
https://doi.org/10.1034/j.1399-0004.1999.550202-3.x
Autor:
Me Suzanne Lewis
Publikováno v:
Clinical Genetics. 55:80-81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f15d4ba470f6d6fdc7827b7112f43bbc
https://doi.org/10.1034/j.1399-0004.1999.550202-1.x
https://doi.org/10.1034/j.1399-0004.1999.550202-1.x
Autor:
Me Suzanne Lewis
Publikováno v:
Clinical Genetics. 55:81-82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2698daeb94621a2bf7dc41cd8ac333c0
https://doi.org/10.1034/j.1399-0004.1999.550202-2.x
https://doi.org/10.1034/j.1399-0004.1999.550202-2.x
Autor:
Me Suzanne Lewis
Publikováno v:
Clinical Genetics. 55:80-80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f936f5a648cd8c2b0827c2f99e234adc
https://doi.org/10.1034/j.1399-0004.1999.550202.x
https://doi.org/10.1034/j.1399-0004.1999.550202.x
Autor:
Wang P; Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, Canada., Carrion P, Qiao Y, Tyson C, Hrynchak M, Calli K, Lopez-Rangel E, Andrieux J, Delobel B, Duban-Bedu B, Thuresson AC, Annerén G, Liu X, Rajcan-Separovic E, Suzanne Lewis ME
Publikováno v:
European journal of medical genetics [Eur J Med Genet] 2013 Aug; Vol. 56 (8), pp. 420-5. Date of Electronic Publication: 2013 May 29.
Autor:
Patel MS; Department of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada., Taylor GP, Bharya S, Al-Sanna'a N, Adatia I, Chitayat D, Suzanne Lewis ME, Human DG
Publikováno v:
American journal of medical genetics. Part A [Am J Med Genet A] 2004 Sep 01; Vol. 129A (3), pp. 294-9.