Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
- DOI
- 10.1186/1471-2350-12-45
- Published
- 2011-03-26
- Container
- BMC Medical Genetics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
Credibility signals
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Cite this work
BibTeX
@article{allodium:10.1186/1471-2350-12-45,
title = {Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene},
author = {Mohammad M Ghahramani Seno and Benjamin YM Kwan and Ka Ki M Lee-Ng and Rainald Moessner and Anath C Lionel and Christian R Marshall and Stephen W Scherer},
year = {2011},
journal = {BMC Medical Genetics},
doi = {10.1186/1471-2350-12-45},
url = {https://doi.org/10.1186/1471-2350-12-45}
}RIS
TY - JOUR TI - Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene AU - Mohammad M Ghahramani Seno AU - Benjamin YM Kwan AU - Ka Ki M Lee-Ng AU - Rainald Moessner AU - Anath C Lionel AU - Christian R Marshall AU - Stephen W Scherer PY - 2011 JO - BMC Medical Genetics DO - 10.1186/1471-2350-12-45 UR - https://doi.org/10.1186/1471-2350-12-45 ER -
APA
Seno, M. M. G., Kwan, B. Y., Lee-Ng, K. K. M., Moessner, R., Lionel, A. C., Marshall, C. R., & Scherer, S. W. (2011). Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene. BMC Medical Genetics. https://doi.org/10.1186/1471-2350-12-45
Source records
- crossref · retrieved 2026-09-26T12:28:04.902Z