Výsledky vyhledávání - Denise Williams
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Changes in the male voice at puberty Autor Meredydd Harries, Jacqueline Walker, Denise Williams, Sarah Hawkins, Ieuan A. Hughes
Vydáno 1997Artigo -
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Randomized Comparison of Epoetin Alfa (40,000 U Weekly) and Darbepoetin Alfa (200 μg Every 2 Weeks) in Anemic Patients with Cancer Receiving Chemotherapy Autor Roger J. Waltzman, C. Croot, Glen R. Justice, Mark R. Fesen, Veena Charu, Denise Williams
Vydáno 2005Artigo -
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Safety assessment of intensive induction therapy in childhood anaplastic large cell lymphoma: Report of the ALCL99 randomised trial Autor Grażyna Wróbel, Audrey Mauguen, Angelo Rosolen, Alfred Reiter, Denise Williams, Keizo Horibe, Laurence Brugières, Marie‐Cécile Le Deley
Vydáno 2011Artigo -
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Prognostic factors in childhood anaplastic large cell lymphoma: results of a large European intergroup study Autor Marie‐Cécile Le Deley, Alfred Reiter, Denise Williams, Georges Delsol, Ilske Oschlies, Keith McCarthy, Martin Zimmermann, Laurence Brugières
Vydáno 2007Artigo -
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Non‐invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosage Autor Michael Parks, Samantha Court, Siobhán Cleary, Samuel Clokie, Julie Hewitt, Denise Williams, Trevor Cole, Fiona MacDonald, Mike Griffiths, Stephanie Allen
Vydáno 2016Artigo -
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Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage Autor Michael Parks, Samantha Court, Benjamin Bowns, Siobhán Cleary, Samuel Clokie, Julie Hewitt, Denise Williams, Trevor Cole, Fiona MacDonald, Mike Griffiths, Stephanie Allen
Vydáno 2017Artigo -
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Impact of the Methotrexate Administration Dose on the Need for Intrathecal Treatment in Children and Adolescents With Anaplastic Large-Cell Lymphoma: Results of a Randomized Trial... Autor Laurence Brugières, Marie‐Cécile Le Deley, Angelo Rosolen, Denise Williams, Keizo Horibe, Grażyna Wróbel, Georg Mann, József Zsíros, Anne Uyttebroeck, Ildikó Márky, Laurence Lamant, Alfred Reiter
Vydáno 2009Artigo -
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Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis Autor Sarah Hillman, Dominic McMullan, Gillian C. Hall, Fiona S. Togneri, James Nuttall, E. J. Maher, César Meller, Denise Williams, Ronald J. Wapner, Eamonn R. Maher, Mark D. Kilby
Vydáno 2013Revisão -
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Risk Factors for Severe Renal Disease in Bardet–Biedl Syndrome Autor Elizabeth Forsythe, Kathryn Sparks, Sunayna Best, Sarah Borrows, Bethan E. Hoskins, Ataf Sabir, Timothy Barrett, Denise Williams, Shehla Mohammed, David Goldsmith, David V. Milford, Detlef Böckenhauer, Lukas Foggensteiner, Philip L. Beales
Vydáno 2016Artigo -
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Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies Autor E Quinlan-Jones, Jenny Lord, Denise Williams, S. Hamilton, Tamás Marton, Ruth Y. Eberhardt, Gabriele Rinck, Elena Prigmore, Rebecca Keelagher, Dominic McMullan, Eamonn R. Maher, Matthew E. Hurles, Mark D. Kilby
Vydáno 2018Artigo
Vyhledávací nástroje:
Související témata
Medicine
Biology
Genetics
Gene
Internal medicine
Mutation
Pediatrics
Phenotype
Fetus
Pathology
Pregnancy
Cohort
Exome sequencing
Prenatal diagnosis
Chemotherapy
Exome
Gastroenterology
Lymphoma
Oncology
Bioinformatics
Endocrinology
Intellectual disability
Missense mutation
Obstetrics
Proband
Psychiatry
Surgery
Cancer
Cancer research
Genetic counseling