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American Journal of Medical Genetics. Part A|April 6, 2011
Three sibs with microcephaly, clubfeet and agenesis of corpus callosum: a new genetic syndrome?Vered Shkalim, Liat Ben-Sira, Dov Inbar, et al.European Journal of Human Genetics : EJHG|November 9, 2006
Allele dosage-dependent penetrance of RET proto-oncogene in an Israeli-Arab inbred family segregating Hirschsprung diseaseLina Basel-Vanagaite, Anna Pelet, Zvi Steiner, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|March 21, 2008
Psychiatric morbidity with focus on obsessive-compulsive disorder in an Israeli cohort of adolescents with mild to moderate mental retardationDoron Gothelf, Olga Goraly, Sari Avni, et al.Journal of Child Neurology|January 8, 2011
An emerging 1q21.1 deletion-associated neurodevelopmental phenotypeLina Basel-Vanagaite, Hadassa Goldberg-Stern, Aviva Mimouni-Bloch, et al.Genetic Testing|February 27, 2008
Genetic carrier screening for spinal muscular atrophy and spinal muscular atrophy with respiratory distress 1 in an isolated population in IsraelLina Basel-Vanagaite, Ellen Taub, Valerie Drasinover, et al.Prenatal Diagnosis|July 1, 2006
Amniotic trisomy 11 mosaicism--is it a benign finding?Lina Basel-Vanagaite, Bella Davidov, Jane Friedman, et al.The Journal of Clinical Endocrinology and Metabolism|July 26, 2014
Exome sequencing reveals SYCE1 mutation associated with autosomal recessive primary ovarian insufficiencyLiat de Vries, Doron M Behar, Pola Smirin-Yosef, et al.American Journal of Medical Genetics. Part A|May 16, 2003
New syndrome of simplified gyral pattern, micromelia, dysmorphic features and early deathLina Basel-Vanagaite, Nufar Marcus, Gil Klinger, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 5, 2011
Phenotypic psychiatric characterization of children with Williams syndrome and response of those with ADHD to methylphenidate treatmentTamar Green, Sarit Avda, Inbar Dotan, et al.Neurogenetics|September 16, 2016
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2ARony Cohen, Ayelet Halevy, Sharon Aharoni, et al.Pageof 8