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Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals

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MICRODELETION, MICRODUPLICATION 22Q11.2, Variable phenotype, Microdeletion syndrome, Chromosome 16p11.2, DISCOVERY, DISORDERS, MICROARRAYS, RETARDATION, LEUKEMIA, POLYMORPHISM

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Citation

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MLA
Bijlsma, EK et al. “Extending the Phenotype of Recurrent Rearrangements of 16p11.2: Deletions in Mentally Retarded Patients Without Autism and in Normal Individuals.” EUROPEAN JOURNAL OF MEDICAL GENETICS 52.2-3 (2009): 77–87. Print.
APA
Bijlsma, E., Gijsbers, A., Schuurs-Hoeijmakers, J., van Haeringen, A., van de Putte, D., Anderlid, B., Lundin, J., et al. (2009). Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. EUROPEAN JOURNAL OF MEDICAL GENETICS, 52(2-3), 77–87.
Chicago author-date
Bijlsma, EK, ACJ Gijsbers, JHM Schuurs-Hoeijmakers, A van Haeringen, DEF van de Putte, BM Anderlid, J Lundin, et al. 2009. “Extending the Phenotype of Recurrent Rearrangements of 16p11.2: Deletions in Mentally Retarded Patients Without Autism and in Normal Individuals.” European Journal of Medical Genetics 52 (2-3): 77–87.
Chicago author-date (all authors)
Bijlsma, EK, ACJ Gijsbers, JHM Schuurs-Hoeijmakers, A van Haeringen, DEF van de Putte, BM Anderlid, J Lundin, P Lapunzina, LAP Jurado, BARBARA DELLE CHIAIE, Bart Loeys, Björn Menten, Ann Oostra, HELENE VERHELST, DJ Amor, DL Bruno, AJ van Essen, R Hordijk, B Sikkema-Raddatz, KT Verbruggen, MCJ Jongmans, R Pfundt, HM Reeser, MH Breuning, and CAL Ruivenkamp. 2009. “Extending the Phenotype of Recurrent Rearrangements of 16p11.2: Deletions in Mentally Retarded Patients Without Autism and in Normal Individuals.” European Journal of Medical Genetics 52 (2-3): 77–87.
Vancouver
1.
Bijlsma E, Gijsbers A, Schuurs-Hoeijmakers J, van Haeringen A, van de Putte D, Anderlid B, et al. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals. EUROPEAN JOURNAL OF MEDICAL GENETICS. 2009;52(2-3):77–87.
IEEE
[1]
E. Bijlsma et al., “Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals,” EUROPEAN JOURNAL OF MEDICAL GENETICS, vol. 52, no. 2–3, pp. 77–87, 2009.
@article{856878,
  author       = {Bijlsma, EK and Gijsbers, ACJ and Schuurs-Hoeijmakers, JHM and van Haeringen, A and van de Putte, DEF and Anderlid, BM and Lundin, J and Lapunzina, P and Jurado, LAP and DELLE CHIAIE, BARBARA and Loeys, Bart and Menten, Björn and Oostra, Ann and Verhelst, Helene and Amor, DJ and Bruno, DL and van Essen, AJ and Hordijk, R and Sikkema-Raddatz, B and Verbruggen, KT and Jongmans, MCJ and Pfundt, R and Reeser, HM and Breuning, MH and Ruivenkamp, CAL},
  issn         = {1769-7212},
  journal      = {EUROPEAN JOURNAL OF MEDICAL GENETICS},
  keywords     = {MICRODELETION,MICRODUPLICATION 22Q11.2,Variable phenotype,Microdeletion syndrome,Chromosome 16p11.2,DISCOVERY,DISORDERS,MICROARRAYS,RETARDATION,LEUKEMIA,POLYMORPHISM},
  language     = {eng},
  number       = {2-3},
  pages        = {77--87},
  title        = {Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals},
  url          = {http://dx.doi.org/10.1016/j.ejmg.2009.03.006},
  volume       = {52},
  year         = {2009},
}

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