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Publications by Chellat Djalila

Screening for the Homozygous C.144delc Mutation in Aurkc Gene in Algerian Infertile Men

Asian Journal of Pharmaceutical and Clinical Research

Pharmaceutical Science

English

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Y Chromosome Microdeletions Screening in Tunisian Infertile Men

Annales de Biologie Clinique

Molecular Biology

English

Mediterranean Fever Gene Mutation Analysis in Infertile Turkish Males

Genetics and Molecular Research

Molecular Biology

English

Novel Homozygous Mutation in the MYO15A Gene in Autosomal Recessive Hearing Loss

Zahedan Journal of Research in Medical Sciences

English

Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.

Journal of Medical Genetics

English

Congenital Central Hypothyroidism Due to a Homozygous Mutation in theTSHβSubunit Gene

Case Reports in Pediatrics

English

Neonatal Cardiomyopathy in Mice Homozygous for the Arg403Gln Mutation in the Α Cardiac Myosin Heavy Chain Gene

Journal of Clinical Investigation

English

Clinical Studies and Thrombin Generation in Patients Homozygous or Heterozygous for the G20210A Mutation in the Prothrombin Gene

Arteriosclerosis, Thrombosis, and Vascular Biology

Cardiovascular Medicine

English

The Higher Risk for Sperm DNA Damage in Infertile Men

Ginekologia Polska

English

1034 a Hypotonic Infant With Methylene Tetrahydrofolate Reductase (MTHFR) Deficiency; Homozygous Mutation of C.1015T>G in MTFHR Gene

Archives of Disease in Childhood

English