A citation-based method for searching scientific literature

Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich, Marie McDonald, Lindsey Campbell, Jeffrey E Ming, Elaine H Zackai, Bassem A Bejjani, Lisa G Shaffer. Mol Cytogenet 2008
Times Cited: 162



Feng Li, Emily C Lisi, Elizabeth S Wohler, Ada Hamosh, Denise A S Batista. Eur J Med Genet 2009
Times Cited: 24




List of shared articles



Times cited

Prenatal detection of a 3q29 microdeletion in a fetus with ventricular septum defect: A case report and literature review.
Fagui Yue, Shu Deng, Qi Xi, Yuting Jiang, Jing He, Hongguo Zhang, Ruizhi Liu. Medicine (Baltimore) 2021
0

Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care.
Rossana Sanchez Russo, Michael J Gambello, Melissa M Murphy, Katrina Aberizk, Emily Black, T Lindsey Burrell, Grace Carlock, Joseph F Cubells, Michael T Epstein, Roberto Espana,[...]. Genet Med 2021
4

Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report.
Melissa M Murphy, T Lindsey Burrell, Joseph F Cubells, Michael T Epstein, Roberto Espana, Michael J Gambello, Katrina Goines, Cheryl Klaiman, Sookyong Koh, Rossana Sanchez Russo,[...]. BMC Psychiatry 2020
3


Familial inheritance of the 3q29 microdeletion syndrome: case report and review.
Wahab A Khan, Ninette Cohen, Stuart A Scott, Elaine M Pereira. BMC Med Genomics 2019
5

Novel 3q27.2-qter deletion in a patient with Diamond-Blackfan anemia and immunodeficiency: Case report and review of literature.
Ebba Alkhunaizi, Brett Schrewe, Reza Alizadehfar, Catherine Vézina, Grant S Stewart, Nancy Braverman. Am J Med Genet A 2017
3



3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.
Santina Città, Serafino Buono, Donatella Greco, Concetta Barone, Enrico Alfei, Sara Bulgheroni, Arianna Usilla, Chiara Pantaleoni, Corrado Romano. Am J Med Genet A 2013
12

A case of 3q29 microdeletion syndrome involving oral cleft inherited from a nonaffected mosaic parent: molecular analysis and ethical implications.
Aline L Petrin, Sandra Daack-Hirsch, Jamie L'Heureux, Jeffrey C Murray. Cleft Palate Craniofac J 2011
7

The 3q29 microdeletion syndrome: report of three new unrelated patients and in silico "RNA binding" analysis of the 3q29 region.
Majed J Dasouki, Gerald H Lushington, Karine Hovanes, James Casey, Mereceds Gorre. Am J Med Genet A 2011
13