Hershkovitz E

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References (2)

Title : The 2p21 deletion syndrome: characterization of the transcription content - Parvari_2005_Genomics_86_195
Author(s) : Parvari R , Gonen Y , Alshafee I , Buriakovsky S , Regev K , Hershkovitz E
Ref : Genomics , 86 :195 , 2005
Abstract : Parvari_2005_Genomics_86_195
ESTHER : Parvari_2005_Genomics_86_195
PubMedSearch : Parvari_2005_Genomics_86_195
PubMedID: 15913950
Gene_locus related to this paper: human-PREPL

Title : A recessive contiguous gene deletion of chromosome 2p16 associated with cystinuria and a mitochondrial disease - Parvari_2001_Am.J.Hum.Genet_69_869
Author(s) : Parvari R , Brodyansky I , Elpeleg O , Moses S , Landau D , Hershkovitz E
Ref : American Journal of Human Genetics , 69 :869 , 2001
Abstract : Parvari_2001_Am.J.Hum.Genet_69_869
ESTHER : Parvari_2001_Am.J.Hum.Genet_69_869
PubMedSearch : Parvari_2001_Am.J.Hum.Genet_69_869
PubMedID: 11524703
Gene_locus related to this paper: human-PREPL