(Q44792425)

6 December 2017

Primary familial congenital erythrocytosis: two novel EPOR mutations found in Spain (English)

1 reference

6 December 2017

Maria Leticia Ribeiro

series ordinal

4

1 reference

6 December 2017

C Bento

1

0 references

author name string

H Almeida

series ordinal

2

1 reference

PubMed ID

23521759

6 December 2017

C Fernandez-Lago

series ordinal

3

1 reference

6 December 2017

22 March 2013

1 reference

International Journal of Laboratory Hematology

6 December 2017

1 reference

6 December 2017

35

1 reference

6 December 2017

5

1 reference

6 December 2017

e27-8

1 reference

The complete evaluation of erythrocytosis: congenital and acquired

6 December 2017

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12061

Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12061

Genetic heterogeneity of primary familial and congenital polycythemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12061

LOVD: easy creation of a locus-specific sequence variation database using an "LSDB-in-a-box" approach

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12061

Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12061

The cytoplasmic region of the erythropoietin receptor contains nonoverlapping positive and negative growth-regulatory domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12061

Molecular genetic analyses in familial and sporadic congenital primary erythrocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FIJLH.12061

21 January 2018

Identifiers

DOI

10.1111/IJLH.12061

1 reference

6 December 2017

1 reference

PubMed ID

23521759