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American Journal of Medical Genetics. Part A|January 19, 2008
Yunis-Varon syndrome: further delineation of the phenotypeLina Basel-Vanagaite, Liora Kornreich, Ofer Schiller, et al.American Journal of Medical Genetics. Part A|August 6, 2008
Autosomal dominant isolated question mark earVered Shkalim, Noam Eliaz, Nehama Linder, et al.American Journal of Medical Genetics|October 26, 2002
Branchial cyst, sensorineural deafness, congenital heart defect, and skeletal abnormalities: Branchio-oto-cardio-skeletal (BOCS) syndrome?Lina Basel-Vanagaite, Mordechai Shohat, Yevgenia Udler, et al.American Journal of Medical Genetics. Part A|January 27, 2010
Acute lymphoblastic leukemia in Weaver syndromeLina Basel-VanagaitePediatric Neurology|August 5, 2010
Clinical and brain imaging heterogeneity of severe microcephalyLina Basel-Vanagaite, William B DobynsPediatric Dermatology|October 15, 2011
New syndrome of congenital circumferential skin folds associated with multiple congenital anomaliesLina Basel-Vanagaite, Eli Sprecher, Andrea Gat, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 18, 2015
A de-novo interstitial microduplication involving 2p16.1-p15 and mirroring 2p16.1-p15 microdeletion syndrome: Clinical and molecular analysisAviva Mimouni-Bloch, Josepha Yeshaya, Sarit Kahana, et al.The Journal of Pediatrics|September 18, 2010
A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromesOmer Zarchi, Josef Attias, Eyal Raveh, et al.American Journal of Medical Genetics. Part A|July 10, 2007
Autosomal recessive mental retardation syndrome with anterior maxillary protrusion and strabismus: MRAMS syndromeLina Basel-Vanagaite, Limor Rainshtein, Dov Inbar, et al.Journal of Child Neurology|July 6, 2005
Familial cognitive impairment with ataxia with oculomotor apraxiaMuhammad Mahajnah, Lina Basel-Vanagaite, Dov Inbar, et al.Pageof 14