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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

372 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
A novel chromosome 19p13.12 deletion in a child with multiple congenital anomalies.
Jensen DR, Martin DM, Gebarski S, Sahoo T, Brundage EK, Chinault AC, Otto EA, Chaki M, Hildebrandt F, Cheung SW, Lesperance MM. Jensen DR, et al. Among authors: martin dm. Am J Med Genet A. 2009 Mar;149A(3):396-402. doi: 10.1002/ajmg.a.32691. Am J Med Genet A. 2009. PMID: 19215039 Free PMC article.
Duplication 16p11.2 in a child with infantile seizure disorder.
Bedoyan JK, Kumar RA, Sudi J, Silverstein F, Ackley T, Iyer RK, Christian SL, Martin DM. Bedoyan JK, et al. Among authors: martin dm. Am J Med Genet A. 2010 Jun;152A(6):1567-74. doi: 10.1002/ajmg.a.33415. Am J Med Genet A. 2010. PMID: 20503337 Free PMC article.
Disruption of RAB40AL function leads to Martin--Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder.
Bedoyan JK, Schaibley VM, Peng W, Bai Y, Mondal K, Shetty AC, Durham M, Micucci JA, Dhiraaj A, Skidmore JM, Kaplan JB, Skinner C, Schwartz CE, Antonellis A, Zwick ME, Cavalcoli JD, Li JZ, Martin DM. Bedoyan JK, et al. Among authors: martin dm. J Med Genet. 2012 May;49(5):332-40. doi: 10.1136/jmedgenet-2011-100575. J Med Genet. 2012. PMID: 22581972 Free PMC article.
Duplication 2p25 in a child with clinical features of CHARGE syndrome.
Sperry ED, Schuette JL, van Ravenswaaij-Arts CM, Green GE, Martin DM. Sperry ED, et al. Among authors: martin dm. Am J Med Genet A. 2016 May;170A(5):1148-54. doi: 10.1002/ajmg.a.37592. Epub 2016 Feb 6. Am J Med Genet A. 2016. PMID: 26850571 Free PMC article.
The impact of serotonin transporter (5-HTTLPR) genotype on the development of resting-state functional connectivity in children and adolescents: a preliminary report.
Wiggins JL, Bedoyan JK, Peltier SJ, Ashinoff S, Carrasco M, Weng SJ, Welsh RC, Martin DM, Monk CS. Wiggins JL, et al. Among authors: martin dm. Neuroimage. 2012 Feb 1;59(3):2760-70. doi: 10.1016/j.neuroimage.2011.10.030. Epub 2011 Oct 18. Neuroimage. 2012. PMID: 22032950 Free PMC article.
372 results