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There are 8010980 results for: content related to: Corrigendum to “The Learning Disabilities Network (LeaDNet): Using Neurofibromatosis Type 1 [NF1] as a Paradigm for Translational Research”

  1. The Learning Disabilities Network (LeaDNet): Using neurofibromatosis type 1 (NF1) as a paradigm for translational research

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 9, September 2012, Pages: 2225–2232, Maria T. Acosta, Carrie E. Bearden, Xavier F. Castellanos, Laurie Cutting, Ype Elgersma, Gerard Gioia, David H. Gutmann, Yong-Seok Lee, Eric Legius, Maximillian Muenke, Kathryn North, Luis F. Parada, Nancy Ratner, Kim Hunter-Schaedle and Alcino J. Silva

    Version of Record online : 20 JUL 2012, DOI: 10.1002/ajmg.a.35535

  2. Reply to the letter to the editor by Szudek et al.—“Growth charts for young children with neurofibromatosis 1 (NF1)”

    American Journal of Medical Genetics

    Volume 92, Issue 3, 29 May 2000, Page: 228, Maurizio Clementi and Romano Tenconi

    Version of Record online : 22 MAY 2000, DOI: 10.1002/(SICI)1096-8628(20000529)92:3<228::AID-AJMG13>3.0.CO;2-4

  3. A cost savings approach to SPRED1 mutational analysis in individuals at risk for neurofibromatosis type 1

    American Journal of Medical Genetics Part A

    Volume 161, Issue 3, March 2013, Pages: 467–472, Talia M. Muram, David A. Stevenson, Sarah Watts-Justice, David H. Viskochil, John C. Carey, Rong Mao and Brian Jackson

    Version of Record online : 7 FEB 2013, DOI: 10.1002/ajmg.a.35718

  4. A novel 5-bp deletion in exon 30 of the neurofibromatosis type 1 (NF1) gene

    Human Mutation

    Volume 13, Issue 3, 1999, Page: 259, Anja Harder, Carmen Macsuga, Sigrid Tinschert, Peter Nürnberg and Hartmut Peters

    Version of Record online : 6 APR 1999, DOI: 10.1002/(SICI)1098-1004(1999)13:3<259::AID-HUMU19>3.0.CO;2-T

  5. Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/−) stem cells

    Human Mutation

    Volume 33, Issue 3, March 2012, Pages: 541–550, Angelika C. Roehl, Tanja Mussotter, David N. Cooper, Lan Kluwe, Katharina Wimmer, Josef Högel, Marion Zetzmann, Julia Vogt, Victor-Felix Mautner and Hildegard Kehrer-Sawatzki

    Version of Record online : 23 JAN 2012, DOI: 10.1002/humu.22013

  6. Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type-3 NF1 deletions

    Human Mutation

    Volume 33, Issue 2, February 2012, Pages: 372–383, Antje M. Zickler, Stephanie Hampp, Ludwine Messiaen, Kathrin Bengesser, Tanja Mussotter, Angelika C. Roehl, Katharina Wimmer, Victor-Felix Mautner, Lan Kluwe, Meena Upadhyaya, Eric Pasmant, Nadia Chuzhanova, Hans A. Kestler, Josef Högel, Eric Legius, Kathleen Claes, David N. Cooper and Hildegard Kehrer-Sawatzki

    Version of Record online : 9 DEC 2011, DOI: 10.1002/humu.21644

  7. Characterization of the somatic mutational spectrum of the neurofibromatosis type 1 (NF1) gene in neurofibromatosis patients with benign and malignant tumors

    Human Mutation

    Volume 23, Issue 2, February 2004, Pages: 134–146, Meena Upadhyaya, Song Han, Claudia Consoli, Elisa Majounie, Martin Horan, Nick S. Thomas, Christopher Potts, Sian Griffiths, Martino Ruggieri, Andreas von Deimling and David N. Cooper

    Version of Record online : 24 DEC 2003, DOI: 10.1002/humu.10305

  8. Index to Volume 7

    Journal of the Royal Anthropological Institute

    Volume 7, Issue 4, December 2001, Pages: 831–841,

    Version of Record online : 20 DEC 2002, DOI: 10.1111/1467-9655.00094

  9. You have free access to this content
    Clean Soil Air Water. 12/2012

    CLEAN – Soil, Air, Water

    Volume 40, Issue 12, December 2012,

    Version of Record online : 4 DEC 2012, DOI: 10.1002/clen.201290024

  10. Letters to the Editor

    Dermatologic Surgery

    Volume 25, Issue 3, March 1999, Pages: 256–258,

    Version of Record online : 24 DEC 2001, DOI: 10.1046/j.1524-4725.1999.025003256.x

  11. Prenatal diagnosis of neurofibromatosis type 1: From flanking rflps to intragenic microsatellite markers

    Prenatal Diagnosis

    Volume 15, Issue 2, February 1995, Pages: 129–134, Conxi Lazaro, Antonia Gaona, Anna Ravella, Victor Volpini and Dr. Xavier Estivill

    Version of Record online : 14 DEC 2005, DOI: 10.1002/pd.1970150204

  12. Assessment of the potential pathogenicity of missense mutations identified in the GTPase-activating protein (GAP)-related domain of the neurofibromatosis type-1 (NF1) gene

    Human Mutation

    Volume 33, Issue 12, December 2012, Pages: 1687–1696, Laura Thomas, Mark Richards, Matthew Mort, Elaine Dunlop, David N. Cooper and Meena Upadhyaya

    Version of Record online : 6 AUG 2012, DOI: 10.1002/humu.22162

  13. Analysis of neurofibromatosis 1 (NF1) lesions by body segment

    American Journal of Medical Genetics Part A

    Volume 125A, Issue 2, 1 March 2004, Pages: 157–161, Chana Palmer, Jacek Szudek, Harry Joe, Vincent M. Riccardi and J.M. Friedman

    Version of Record online : 24 JUN 2003, DOI: 10.1002/ajmg.a.20354

  14. Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumors

    Genes, Chromosomes and Cancer

    Volume 51, Issue 5, May 2012, Pages: 429–437, Douglas R. Stewart, Alexander Pemov, Peter Van Loo, Eline Beert, Hilde Brems, Raf Sciot, Kathleen Claes, Evgenia Pak, Amalia Dutra, Chyi-Chia Richard Lee and Eric Legius

    Version of Record online : 17 JAN 2012, DOI: 10.1002/gcc.21928

  15. Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome

    American Journal of Medical Genetics

    Volume 75, Issue 3, 23 January 1998, Pages: 265–272, Michel Bahuau, Claude Houdayer, Brigitte Assouline, Claudine Blanchet-Bardon, Martine Le Merrer, Stanislas Lyonnet, Sophie Giraud, Dominique Récan, Hakima Lakhdar, Michel Vidaud and Dominique Vidaud

    Version of Record online : 6 DEC 1998, DOI: 10.1002/(SICI)1096-8628(19980123)75:3<265::AID-AJMG8>3.0.CO;2-P

  16. Analysis of intrafamilial phenotypic variation in neurofibromatosis 1 (NF1)

    Genetic Epidemiology

    Volume 23, Issue 2, August 2002, Pages: 150–164, J. Szudek, H. Joe and J.M. Friedman

    Version of Record online : 3 SEP 2002, DOI: 10.1002/gepi.1129

  17. Neurofibromatosis type 1: A model condition for the study of the molecular basis of variable expressivity in human disorders

    American Journal of Medical Genetics

    Volume 89, Issue 1, 26 March 1999, Pages: 7–13, John C. Carey and David H. Viskochil

    Version of Record online : 30 AUG 1999, DOI: 10.1002/(SICI)1096-8628(19990326)89:1<7::AID-AJMG4>3.0.CO;2-#

  18. The heterogeneous nature of germline mutations in NF1 patients with malignant peripheral serve sheath tumours (MPNSTs)

    Human Mutation

    Volume 27, Issue 7, July 2006, Page: 716, Meena Upadhyaya, Gill Spurlock, Elisa Majounie, Sian Griffiths, Natalie Forrester, Mike Baser, Susan M. Huson, D. Gareth Evans and Rosalie Ferner

    Version of Record online : 19 JUN 2006, DOI: 10.1002/humu.9429

  19. Contents

    Congenital Anomalies

    Volume 44, Issue 4, December 2004, Pages: J56–J57,

    Version of Record online : 3 DEC 2004, DOI: 10.1111/j.1741-4520.2004.00051.x

  20. Bilateral (opercular and paracentral lobular) polymicrogyria and neurofibromatosis type 1

    American Journal of Medical Genetics Part A

    Volume 155, Issue 3, March 2011, Pages: 582–585, Martino Ruggieri, Mario Mastrangelo, Alberto Spalice, Rosanna Mariani, Isabella Torrente, Agata Polizzi, Irene Bottillo, Claudio Di Biase and Paola Iannetti

    Version of Record online : 22 FEB 2011, DOI: 10.1002/ajmg.a.33318