36672838 34488710 37009284 35892614 - Search Results

Save citations to file

Email citations

Your saved search

Your RSS Feed

Year	Number of Results
2021	1
2022	2
2023	1

Page 1

Analysis of SNHG14: A Long Non-Coding RNA Hosting SNORD116, Whose Loss Contributes to Prader-Willi Syndrome Etiology.

Ariyanfar S, Good DJ. Ariyanfar S, et al. Genes (Basel). 2022 Dec 29;14(1):97. doi: 10.3390/genes14010097. Genes (Basel). 2022. PMID: 36672838 Free PMC article. Review.

Suicidality in individuals with Prader-Willi syndrome: a review of registry survey data.

Peleggi A, Bohonowych J, Strong TV, Schwartz L, Kim SJ. Peleggi A, et al. BMC Psychiatry. 2021 Sep 6;21(1):438. doi: 10.1186/s12888-021-03436-3. BMC Psychiatry. 2021. PMID: 34488710 Free PMC article. Review.

Case report: Prader-Willi syndrome and inflammatory arthritis-An important consideration.

Marelli L, Dallos T, Miserocchi E, Nucci P, Tombolini B, De Lucia O, Gattinara M, Caporali R, Marino A. Marelli L, et al. Front Pediatr. 2023 Mar 17;11:1102382. doi: 10.3389/fped.2023.1102382. eCollection 2023. Front Pediatr. 2023. PMID: 37009284 Free PMC article.

Development of an International Database for a Rare Genetic Disorder: The MECP2 Duplication Database (MDBase).

Ta D, Downs J, Baynam G, Wilson A, Richmond P, Schmidt A, Decker A, Leonard H. Ta D, et al. Children (Basel). 2022 Jul 25;9(8):1111. doi: 10.3390/children9081111. Children (Basel). 2022. PMID: 35892614 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

4 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

4 results

Results by year