Zobrazeno 1 - 10
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pro vyhledávání: '"betha thalassemia"'
Akademický článek
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Autor:
Blanca Issé, Myriam E. Ledesma Achem, Sandra Stella Lazarte, Ana Cecilia Haro, Maria Eugenia Monaco, Cecilia Jiménez
Publikováno v:
Hemoglobin. 38:394-401
The main hereditary hemoglobin (Hb) disorder in Argentina is b-thalassemia (b-thal). Molecular studies performed in the center of the country exhibited a marked prevalence of the codon 39 (C4T) and IVS-I-110 (G4A) mutations. The northwest region of A
Autor:
Balcázar-Villarroel, Mario1 (AUTHOR) informaciones.tecnomedic@gmail.com, Mancilla-Uribe, Angélica1 (AUTHOR) sandra.navia@gmail.com, Navia-León, Sandra1 (AUTHOR), Carmine, Florencia2 (AUTHOR) f.carmine02@ufromail.cl, Birditt, Katherine3 (AUTHOR) krb56@cam.ac.uk, Sandoval, Cristian4,5,6 (AUTHOR) mariobalcazar91@gmail.com
Publikováno v:
Diagnostics (2075-4418). Nov2024, Vol. 14 Issue 21, p2353. 16p.
Publikováno v:
Human Reproduction Update; May/Jun2021, Vol. 27 Issue 3, p433-459, 27p
Publikováno v:
Human Reproduction; Jan2021, Vol. 36 Issue 1, p26-39, 14p
Autor:
Soteh, Mohammad Bagher Hashemi1, Niaki, Haleh Akhavan2, Kowsarian, Mehrnoosh1, Aliasgharian, Aily1, Banihashemi, Ali2
Publikováno v:
Journal of Mazandaran University of Medical Sciences (JMUMS). 2008, Vol. 18 Issue 67, p1-9. 9p.
Publikováno v:
Annals of Noninvasive Electrocardiology; Jul2016, Vol. 21 Issue 4, p335-342, 8p
Publikováno v:
Internal & Emergency Medicine; Dec2012 Supplement, Vol. 7, p309-359, 51p
Publikováno v:
Journal of Community Genetics; Jul2012, Vol. 3 Issue 3, p221-228, 8p
Autor:
Elisabeth Hildt, Sigrid Graumann
Published in 1999, this book discusses issues related to the current and possible future technological progress in genetic technology linked to in vitro fertilization, specifically preimplantation diagnosis and germline gene therapy, from a scientifi