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American Journal of Medical Genetics|December 31, 1997
Velocardiofacial manifestations and microdeletions in schizophrenic inpatientsD Gothelf, A Frisch, H Munitz, et al.Annals of Human Genetics|March 3, 2007
The fate of 12 recessive mutations in a single villageJ Zlotogora, Y Hujerat, S Barges, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literatureManu S Raam, Benjamin D Solomon, Stavit A Shalev, et al.Child Psychiatry and Human Development|July 28, 1999
Childhood imaginary companionship and mental health in adolescenceO Bonne, L Canetti, E Bachar, et al.Journal of Applied Behavior Analysis|January 10, 2018
Treating liquid expulsion in children with feeding disordersRebecca A Shalev, Suzanne M Milnes, Cathleen C Piazza, et al.Laboratory Investigation; a Journal of Technical Methods and Pathology|May 1, 1993
Wide distribution of granulophysin epitopes in granules of human tissuesL Hatskelzon, B I Dalal, A Shalev, et al.European Journal of Endocrinology|March 17, 2010
ANE syndrome caused by mutated RBM28 gene: a novel etiology of combined pituitary hormone deficiencyRonen Spiegel, Stavit A Shalev, Amin Adawi, et al.American Journal of Medical Genetics. Part A|July 10, 2007
An association of Hutchinson-Gilford progeria and malignancyStavit A Shalev, Annachiara De Sandre-Giovannoli, Ayelet Adir Shani, et al.Journal of Human Genetics|August 23, 2006
Wide clinical spectrum in a family with hereditary lymphedema type I due to a novel missense mutation in VEGFR3Ronen Spiegel, Arash Ghalamkarpour, Etty Daniel-Spiegel, et al.Biological Psychiatry|September 1, 1988
Audiological evaluation of nonalcoholic, drug-free posttraumatic stress disorder patientsA Shalev, J Attias, A Bleich, et al.Pageof 25