Wikidata

(Q36834992)

English

Kostmann syndrome or infantile genetic agranulocytosis, part two: Understanding the underlying genetic defects in severe congenital neutropenia

scientific article published on June 2007

In more languages

Statements

title
Kostmann syndrome or infantile genetic agranulocytosis, part two: Understanding the underlying genetic defects in severe congenital neutropenia (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
17537008
retrieved
16 August 2017
author name string
Göran Carlsson
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
17537008
retrieved
16 August 2017
Malin Melin
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
17537008
retrieved
16 August 2017
Niklas Dahl
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
17537008
retrieved
16 August 2017
Kim Göransdotter Ramme
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
17537008
retrieved
16 August 2017
page(s)
813-819
1 reference
stated in
Europe PubMed Central
PubMed ID
17537008
retrieved
16 August 2017

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit
                    Retrieved from "https://www.wikidata.org/w/index.php?title=Q36834992&oldid=2045255214"