Talk:3q29 microdeletion syndrome

3q29 microdeletion syndrome is within the scope of WikiProject Disability. For more information, visit the project page, where you can join the project and/or contribute to the discussion.DisabilityWikipedia:WikiProject DisabilityTemplate:WikiProject DisabilityDisability articles

Medicine Low‑importance

	Medicine portal This article is within the scope of WikiProject Medicine, which recommends that medicine-related articles follow the Manual of Style for medicine-related articles and that biomedical information in any article use high-quality medical sources. Please visit the project page for details or ask questions at Wikipedia talk:WikiProject Medicine.MedicineWikipedia:WikiProject MedicineTemplate:WikiProject Medicinemedicine articles
Low	This article has been rated as Low-importance on the project's importance scale.

Ideal sources for Wikipedia's health content are defined in the guideline Wikipedia:Identifying reliable sources (medicine) and are typically review articles. Here are links to possibly useful sources of information about 3q29 microdeletion syndrome.

PubMed provides review articles from the past five years (limit to free review articles)
The TRIP database provides clinical publications about evidence-based medicine.
Other potential sources include: Centre for Reviews and Dissemination and CDC

The content of this article has been derived in whole or part from https://decipher.sanger.ac.uk/application/syndrome/. Permission has been received from the copyright holder to release this material . Evidence of this has been confirmed and stored by VRT volunteers, under ticket number 2010060410028871.
This template is used by approved volunteers dealing with the Wikimedia volunteer response team system (VRTS) after receipt of a clear statement of permission at permissions-enwikimedia.org. Do not use this template to claim permission.

Untitled

This article needs substantial revision. There are at least two case studies of children with normal cognitive function. This article doesn't begin to address the great variabilty in phenotype. Cgkleiber (talk) 18:44, 3 November 2011 (UTC)cgkleiber[reply]

William Cobb, Arne Anderson, Clesson Turner, Ruth D. Hoffman, Steven Schonberg, Sondra W. Levin, 1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child, European Journal of Medical Genetics, Volume 53, Issue 6, November-December 2010, Pages 415-418, ISSN 1769-7212, 10.1016/j.ejmg.2010.08.009. (http://www.sciencedirect.com/science/article/pii/S176972121000090X) Keywords: Deletion 3q29; IQ; Autism; Array CGH analysis

Feng Li, Emily C. Lisi, Elizabeth S. Wohler, Ada Hamosh, Denise A.S. Batista, 3q29 interstitial microdeletion syndrome: An inherited case associated with cardiac defect and normal cognition, European Journal of Medical Genetics, Volume 52, Issue 5, September-October 2009, Pages 349-352, ISSN 1769-7212, 10.1016/j.ejmg.2009.05.001. (http://www.sciencedirect.com/science/article/pii/S1769721209000597) Keywords: 3q29; Microdeletion; Microarray; PDA; Cardiac defect

What does this mean: "6 and 9/12-year-old male patient"

A person cannot have two different ages. And the fraction 9/12 seems a silly, wrong way to write "three quarters". 2A00:23C5:FE1C:3701:49D0:1ABA:3934:4EBA (talk) 19:53, 5 November 2024 (UTC)[reply]

I looked at the source and the quote is "Our patient was a 6 and 9/12 year-old male who is the fourth...". I will remove the extra hyphen in our article. 9/12 seems silly to me too, but may be the scientific way to write it. Commander Keane (talk) 05:49, 6 November 2024 (UTC)[reply]