Suchergebnisse - "Norberg, Anna"

PubPharm (10)

1

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations : a pedigree-based measured genotype association analysis

enthalten in: BMC medical genetics | 2017

von Winbo, A. | Stattin, E. | Westin, I. | +4

2

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

enthalten in: BMC medical genetics | 2017

von Winbo, A. | Stattin, E. | Westin, I. | +4

3

Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis

enthalten in: BMC medical genetics | 2017

von Winbo, A. | Stattin, E. | Westin, I. | +4

4

Genetic screening in sudden cardiac death in the young can save future lives

enthalten in: International journal of legal medicine | 2016

von Stattin, E. | Westin, I. | Cederquist, K. | +6

5

Genetic screening in sudden cardiac death in the young can save future lives

enthalten in: International journal of legal medicine | 2015

von Stattin, E. | Westin, I. | Cederquist, K. | +6

6

Genetic screening in sudden cardiac death in the young can save future lives

enthalten in: International journal of legal medicine | 2015

von Stattin, E. | Westin, I. | Cederquist, K. | +6

7

Genetic screening in sudden cardiac death in the young can save future lives

enthalten in: International journal of legal medicine | 2015

von Stattin, E. | Westin, I. | Cederquist, K. | +6

8

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

enthalten in: BMC cardiovascular disorders | 2012

von Stattin, E. | Boström, I. | Winbo, A. | +7

9

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

enthalten in: BMC cardiovascular disorders | 2012

von Stattin, E. | Boström, I. | Winbo, A. | +7

10

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

in: BMC Cardiovascular Disorders | 2012

von Stattin Eva-Lena | Boström Ida | Winbo Annika | +7

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