SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Eva Hladilkova, Tuva Barøy, Madeleine Fannemel, Vladimira Vallova, Doriana Misceo, Vesna Bryn, Iva Slamova, Sarka Prasilova, Petr Kuglik, Eirik Frengen, A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms, Molecular Cytogenetics, 2015, 8, 1

    CrossRef

  2. 2
    Linda Bamonte, Developmental Presentation, Medical Complexities, and Service Delivery for a Child With 16p11.2 Deletion Syndrome, Pediatric Physical Therapy, 2015, 27, 1, 90

    CrossRef

  3. 3
    Merlin Butler, Syed Rafi, Ann Manzardo, High-Resolution Chromosome Ideogram Representation of Currently Recognized Genes for Autism Spectrum Disorders, International Journal of Molecular Sciences, 2015, 16, 3, 6464

    CrossRef

  4. 4
    Kitiwan Rojnueangnit, Fady M. Mikhail, Xiangqin Cui, Shaohua Yu, Nathaniel H. Robin, Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients With Cleft Lip and/or Palate, The Cleft Palate-Craniofacial Journal, 2015, 52, 6, 724

    CrossRef

  5. 5
    Nobuhiko Okamoto, Tatsuya Fujii, Junko Tanaka, Kazumasa Saito, Takeshi Matsui, Naoki Harada, A clinical study of patients with pericentromeric deletion and duplication within 16p12.2–p11.2, American Journal of Medical Genetics Part A, 2014, 164, 1
  6. 6
    John C K Barber, Victoria Hall, Viv K Maloney, Shuwen Huang, Angharad M Roberts, Angela F Brady, Nicki Foulds, Beverley Bewes, Marianne Volleth, Thomas Liehr, Karl Mehnert, Mark Bateman, Helen White, 16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2, European Journal of Human Genetics, 2013, 21, 2, 182

    CrossRef

  7. 7
    Dianne F Newbury, Francesca Mari, Elham Sadighi Akha, Kay D MacDermot, Roberto Canitano, Anthony P Monaco, Jenny C Taylor, Alessandra Renieri, Simon E Fisher, Samantha J L Knight, Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder, European Journal of Human Genetics, 2013, 21, 4, 361

    CrossRef

  8. 8
    Tracy Tucker, Sylvie Giroux, Valérie Clément, Sylvie Langlois, Jan M. Friedman, François Rousseau, Prevalence of selected genomic deletions and duplications in a French–Canadian population-based sample of newborns, Molecular Genetics & Genomic Medicine, 2013, 1, 2
  9. 9
    Rocio Moran, Nathaniel H. Robin, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

    CrossRef

  10. 10
    Merlin G. Butler, Erin L. Youngs, Jennifer L. Roberts, Jessica A. Hellings, Assessment and Treatment in Autism Spectrum Disorders: A Focus on Genetics and Psychiatry, Autism Research and Treatment, 2012, 2012, 1

    CrossRef

  11. 11
    Anne-Claude Tabet, Marion Pilorge, Richard Delorme, Frédérique Amsellem, Jean-Marc Pinard, Marion Leboyer, Alain Verloes, Brigitte Benzacken, Catalina Betancur, Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother, European Journal of Human Genetics, 2012, 20, 5, 540

    CrossRef

  12. 12
    W. Gregory Feero, Alan E. Guttmacher, Heather C. Mefford, Mark L. Batshaw, Eric P. Hoffman, Genomics, Intellectual Disability, and Autism, New England Journal of Medicine, 2012, 366, 8, 733

    CrossRef

  13. 13
    A.M. George, J. Taylor, D.R. Love, Microdeletions in 16p11.2 and 13q31.3 associated with developmental delay and generalized overgrowth, Genetics and Molecular Research, 2012, 11, 3, 3133

    CrossRef

  14. 14
    Maria Descartes, Bruce R. Korf, Fady M. Mikhail, Swaiman's Pediatric Neurology, 2012,

    CrossRef

  15. 15
    Tanya M. Bardakjian, Simon Kwok, Anne M. Slavotinek, Adele S. Schneider, Clinical report of microphthalmia and optic nerve coloboma associated with a de novo microdeletion of chromosome 16p11.2, American Journal of Medical Genetics Part A, 2010, 152A, 12
  16. 16
    Hans Hilger Ropers, Genetics of Early Onset Cognitive Impairment, Annual Review of Genomics and Human Genetics, 2010, 11, 1, 161

    CrossRef

  17. 17
    Surasak Puvabanditsin, Michael S. Nagar, Meera Joshi, George Lambert, Eugene Garrow, Erik Brandsma, Microdeletion of 16p11.2 associated with endocardial fibroelastosis, American Journal of Medical Genetics Part A, 2010, 152A, 9
  18. 18
    Ruxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, Gwen M Glew, Anne V Hing, Stephanie Wallace, Patricia I Bader, Aline Hamati, Pamela J Reitnauer, Rosemarie Smith, David W Stockton, Hiltrud Muhle, Ingo Helbig, Evan E Eichler, Blake C Ballif, Jill Rosenfeld, Karen D Tsuchiya, Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity, Genetics in Medicine, 2010, 12, 10, 641

    CrossRef