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American Journal of Medical Genetics|July 3, 1995
Renal anomalies in Marden-Walker syndrome: a clue for prenatal diagnosisZ Ben-Neriah, S Yagel, I ArielAmerican Journal of Perinatology|March 1, 1993
Survival in an infant with a prenatally diagnosed Meckel syndrome variantM Kaplan, Z Ben-Neriah, R AchironJournal of Inherited Metabolic Disease|November 20, 1998
Variables influencing parental perception of inherited metabolic diseases before and after genetic counsellingR Saleem, R Gofin, Z Ben-Neriah, et al.FEBS Letters|September 5, 1983
Direct measurements of the dextran-dependent calcium uptake by rat peritoneal mast cellsR Sagi-Eisenberg, C Geller-Bernstein, Z Ben-Neriah, et al.Neuropharmacology|February 1, 1983
Structure-activity relationship in the mast cell degranulating capacity of neurotensin fragmentsR Sagi-Eisenberg, Z Ben-Neriah, I Pecht, et al.Clinical Genetics|January 1, 1995
Antley-Bixler syndrome and esophageal atresia in a patient with trisomy 21E Feigin, R Udassin, D Seror, et al.Prenatal Diagnosis|February 1, 1997
Trisomy 2: confined placental mosaicism in a fetus with intrauterine growth retardationI Ariel, I Lerer, S Yagel, et al.Human Mutation|October 23, 2001
A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi JewsI Lerer, M Sagi, Z Ben-Neriah, et al.Journal of Inherited Metabolic Disease|January 14, 1998
Aspartylglucosaminuria among Palestinian ArabsJ Zlotogora, Z Ben-Neriah, B Y Abu-Libdeh, et al.Journal of Medical Genetics|November 14, 1997
A syndrome including thumb malformations, microcephaly, short stature, and hypogonadismJ Zlotogora, J Dagan, A Ganen, et al.Pageof 2