Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.

Balasubramanian M, Smith K, Basel-Vanagaite L, Feingold MF, Brock P, Gowans GC, Vasudevan PC, Cresswell L, Taylor EJ, Harris CJ, Friedman N, Moran R, Feret H, Zackai EH, Theisen A, Rosenfeld JA, Parker MJ

Open source

DOI: 10.1136/jmg.2010.084491
Published: 2011 May
Container: Journal of medical genetics
Publisher: Not recorded
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1136/jmg.2010.084491,
  title = {Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.},
  author = {Balasubramanian M and Smith K and Basel-Vanagaite L and Feingold MF and Brock P and Gowans GC and Vasudevan PC and Cresswell L and Taylor EJ and Harris CJ and Friedman N and Moran R and Feret H and Zackai EH and Theisen A and Rosenfeld JA and Parker MJ},
  year = {2011},
  journal = {Journal of medical genetics},
  doi = {10.1136/jmg.2010.084491},
  url = {https://doi.org/10.1136/jmg.2010.084491}
}

RIS

TY  - JOUR
TI  - Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.
AU  - Balasubramanian M
AU  - Smith K
AU  - Basel-Vanagaite L
AU  - Feingold MF
AU  - Brock P
AU  - Gowans GC
AU  - Vasudevan PC
AU  - Cresswell L
AU  - Taylor EJ
AU  - Harris CJ
AU  - Friedman N
AU  - Moran R
AU  - Feret H
AU  - Zackai EH
AU  - Theisen A
AU  - Rosenfeld JA
AU  - Parker MJ
PY  - 2011
JO  - Journal of medical genetics
DO  - 10.1136/jmg.2010.084491
UR  - https://doi.org/10.1136/jmg.2010.084491
ER  -

APA

M, B., K, S., L, B., MF, F., P, B., GC, G., PC, V., L, C., EJ, T., CJ, H., N, F., R, M., H, F., EH, Z., A, T., JA, R., & MJ, P. (2011). Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotype.. Journal of medical genetics. https://doi.org/10.1136/jmg.2010.084491

Source records

pubmed · retrieved 2026-09-25T18:29:44.716Z