Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 4
2004 2
2005 1
2006 1
2008 1
2009 1
2014 1
2015 2
2018 2
2023 0

Text availability

Article attribute

Article type

Publication date

Search Results

15 results

Results by year

Filters applied: . Clear all
Page 1
Advances in Tourette syndrome: diagnoses and treatment.
Serajee FJ, Mahbubul Huq AH. Serajee FJ, et al. Pediatr Clin North Am. 2015 Jun;62(3):687-701. doi: 10.1016/j.pcl.2015.03.007. Epub 2015 Apr 16. Pediatr Clin North Am. 2015. PMID: 26022170 Review.
Homozygous myotonic dystrophy with craniosynostosis.
Cerghet M, Tapos D, Serajee FJ, Mahbubul Huq AH. Cerghet M, et al. Among authors: serajee fj. J Child Neurol. 2008 Aug;23(8):930-3. doi: 10.1177/0883073808314965. Epub 2008 May 12. J Child Neurol. 2008. PMID: 18474935
Association of Y chromosome haplotypes with autism.
Serajee FJ, Mahbubul Huq AH. Serajee FJ, et al. J Child Neurol. 2009 Oct;24(10):1258-61. doi: 10.1177/0883073809333530. Epub 2009 Jul 15. J Child Neurol. 2009. PMID: 19605777
Association of Reelin gene polymorphisms with autism.
Serajee FJ, Zhong H, Mahbubul Huq AH. Serajee FJ, et al. Genomics. 2006 Jan;87(1):75-83. doi: 10.1016/j.ygeno.2005.09.008. Epub 2005 Nov 28. Genomics. 2006. PMID: 16311013 Free article.
Evidence of somatic mosaicism in Sturge-Weber syndrome.
Huq AH, Chugani DC, Hukku B, Serajee FJ. Huq AH, et al. Among authors: serajee fj. Neurology. 2002 Sep 10;59(5):780-2. doi: 10.1212/wnl.59.5.780. Neurology. 2002. PMID: 12221183 No abstract available.
O-GlcNAc transferase missense mutations linked to X-linked intellectual disability deregulate genes involved in cell fate determination and signaling.
Selvan N, George S, Serajee FJ, Shaw M, Hobson L, Kalscheuer V, Prasad N, Levy SE, Taylor J, Aftimos S, Schwartz CE, Huq AM, Gecz J, Wells L. Selvan N, et al. Among authors: serajee fj. J Biol Chem. 2018 Jul 6;293(27):10810-10824. doi: 10.1074/jbc.RA118.002583. Epub 2018 May 16. J Biol Chem. 2018. PMID: 29769320 Free PMC article.
15 results