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  The predominance of codon 39 (c>t) mutation of HBB gene in a portion of the Algerian population (Northeast Algeria)

  Belhadi Kamilia, Yahia Mouloud, Gribaa Moez, Bendaoud Fadhila, Ben Charfeddine Ilhem, Manoubi Wiem

  2017-04-20

  Published: April 20, 2017

  3070

  PDF: 1364
• 

  Kearns-Sayre syndrome with optic nerve atrophy phenotype: A possible biological and clinical concurrence of two mutations?

  Agostino Berio, Gian Luigi Mariottini, Marco Frascio, Attilia Piazzi

  2022-03-01

  Published: March 1, 2022

  1222

  PDF: 290

• USE OF THE AMPLIFICATION REFRACTORY MUTATION SYSTEM (ARMS) IN THE STUDY OF HBS IN PREDYNASTIC EGYPTIAN REMAINS

  A. Marin, N. Cerutti, E. Rabino Massa

  1999-06-30

  Published: June 30, 1999

  103

  PDF: 101

• Preservation and identification of ancient M. tuberculosis complex DNA in Egyptian mummies

  Albert R. Zink, Stephanie Köhler, Nasim Motamedi, Udo Reischl, Hans Wolf, Andreas G. Nerlich

  Published:

  227

  PDF: 190

• Genetic variation in GSTP1 and TBXA2R genes: influence of Badoush cement factory pollutant

  Dema Mohammed Sabah, Mohammad Ibrahim Khalil

  2024-11-21

  Published: November 21, 2024

  0

  PDF: 0