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American Journal of Medical Genetics. Part A|September 15, 2015
A PIGN mutation responsible for multiple congenital anomalies-hypotonia-seizures syndrome 1 (MCAHS1) in an Israeli-Arab familyMorad Khayat, Joseph Mark Tilghman, Ilana Chervinsky, et al.
Infection|April 3, 2007
Conservative management of implantable cardioverter defibrillator-related endocarditis due to Bacillus sppA Shalev, J Gilad, K Riesenberg, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|July 24, 2004
Thrombophilia and stillbirth: possible connection by intrauterine growth restrictionZeev Weiner, Ronit Beck-Fruchter, Amir Weiss, et al.
Developmental and Comparative Immunology|January 1, 1984
Specific activity of carp antisera against beta 2-microglobulin (beta 2m) and evidence for a beta 2m homologue in carp (Cyprinus carpio)A Shalev, R R Caspi, L Lögdberg, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|September 5, 2001
Abnormal thermoregulation in drug-free male schizophrenia patientsR Shiloh, A Weizman, Y Epstein, et al.
European Journal of Human Genetics : EJHG|October 3, 2003
Limb-girdle muscular dystrophy 2I: phenotypic variability within a large consanguineous Bedouin family associated with a novel FKRP mutationTamar Harel, Yael Goldberg, Stavit A Shalev, et al.
NPJ Genomic Medicine|September 24, 2021
MCM9 is associated with germline predisposition to early-onset cancer-clinical evidenceYael Goldberg, Ola Aleme, Lilach Peled-Perets, et al.
The Journal of Clinical Endocrinology and Metabolism|November 4, 2000
Mutations in the steroidogenic acute regulatory protein (StAR) in six patients with congenital lipoid adrenal hyperplasiaH S Bose, S Sato, J Aisenberg, et al.
American Journal of Medical Genetics. Part A|December 15, 2005
Clinical variation of Aarskog syndrome in a large family with 2189delA in the FGD1 geneStavit A Shalev, Elana Chervinski, Ehud Weiner, et al.
American Journal of Human Genetics|July 27, 2010
Autosomal-recessive early-onset retinitis pigmentosa caused by a mutation in PDE6G, the gene encoding the gamma subunit of rod cGMP phosphodiesteraseLiron Dvir, Gassoub Srour, Rasmi Abu-Ras, et al.
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