Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha0-thalassemia deletions - -Mex1and

Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha0-thalassemia deletions - -Mex1and - -Mex2

Published:2016-06-24 Issue:5 Volume:38 Page:535-542
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

de-la-Cruz-Salcedo E. I.¹,Ibarra B.¹,Rizo-de-la-Torre L. C.¹²,Sánchez-López J. Y.¹²,González-Mercado A.¹,Harteveld C. L.³,Perea-Díaz F. J.¹²

Affiliation:

1. Doctorado en Genética Humana; Centro Universitario de Ciencias de la Salud; Universidad de Guadalajara; Guadalajara Jalisco Mexico

2. División de Genética; Centro de Investigación Biomédica de Occidente; Instituto Mexicano del Seguro Social; Guadalajara Jalisco Mexico

3. Human and Clinical Genetics; Leiden University Medical Center; Leiden The Netherlands

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

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4. EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies;Traeger-Synodinos;Eur J Hum Genet,2015

5. A simple salting out procedure for extracting DNA from human nucleated cells;Miller;Nucleic Acids Res,1998

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