Orphanet: Molecular diagnosis of severe congenital neutropenia ELANE, HAX1, GFI1, G6PC3, WAS and CSF3R gene sequencing
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Molecular diagnosis of severe congenital neutropenia (ELANE, HAX1, GFI1, G6PC3, WAS and CSF3R gene sequencing)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 06/08/2010
  • Molecular pediatric hematology laboratory
  • Pediatric hematology - oncology department
  • Schneider Children's Medical Center of Israel
  • 14 Kaplan st.,2nd floor, PO Box 559
  • PETAH TIKVA 49202
  • ISRAEL
  • Director of laboratory : Dr Orly DGANI
  • More information
  • Phone : 972 3 9253669
  • Additional Phone : -
  • Fax : 972 3 9253042
  • Contact
Last update: August 2010

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of diseases tested (1)
Severe congenital neutropenia
List of genes tested (including panels) (6)
CSF3R
ELANE
G6PC3
GFI1
HAX1
WAS
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