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Subject GENETICS

3. Case fatality rate and associated factors in patients with 22q11 microdeletion syndrome: a retrospective cohort study. Issue 11 (6th November 2014)

Authors:
Repetto, Gabriela M; Guzmán, M Luisa; Delgado, Iris; Loyola, Hugo; Palomares, Mirta; Lay-Son, Guillermo; Vial, Cecilia; Benavides, Felipe; Espinoza, Karena; Alvarez, Patricia
Journal:
BMJ open
Issue:
Volume 4:Issue 11(2014)
Page Start:
Record Type:
Journal Article
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6. Novel genotype–phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy. Issue 4 (28th October 2014)

Authors:
Lopes, Luis R; Syrris, Petros; Guttmann, Oliver P; O'Mahony, Constantinos; Tang, Hak Chiaw; Dalageorgou, Chrysoula; Jenkins, Sharon; Hubank, Mike; Monserrat, Lorenzo; McKenna, William J; Plagnol, Vincent; Elliott, Perry M
Journal:
Heart
Issue:
Volume 101:Issue 4(2015)
Page Start:
294
Record Type:
Journal Article
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7. Oestrogen receptor polymorphisms are an associated risk factor for mild cognitive impairment and Alzheimer disease in women APOE ɛ4 carriers: a case–control study. Issue 9 (18th September 2013)

Authors:
Fernández-Martínez, Manuel; Elcoroaristizabal Martín, Xabier; Blanco Martín, Elisa; Galdos Alcelay, Luis; Ugarriza Serrano, Iratxe; Gómez Busto, Fernando; Álvarez-Álvarez, Maite; Molano Salazar, Ana; Bereincua Gandarias, Rocio; Inglés Borda, Sandra; Uterga Valiente, Juan María; Indakoetxea Juanbe...
Journal:
BMJ open
Issue:
Volume 3:Issue 9(2013)
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Record Type:
Journal Article
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8. Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy. Issue 1 (21st July 2014)

Authors:
Wasielewski, Marijke; van Spaendonck-Zwarts, Karin Y; Westerink, Nico-Derk L; Jongbloed, Jan D H; Postma, Aleida; Gietema, Jourik A; van Tintelen, J Peter; van den Berg, Maarten P
Journal:
Open heart
Issue:
Volume 1:Issue 1(2014)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗