Results 111 to 120 of about 1,119,993 (215)

Molecular diagnosis of thalassaemia syndromes

open access: yes, 2001
Thalassaemia syndromes are a group of hereditary disorders in which a defect in the synthesis of globin polypeptide chains of haemoglobin is present. Clinical manifestations are diverse, ranging from asymptomatic hypochromia and microcytosis to profound ...
Pavlović, Sonja
core  

Characterisation of Urine-Derived Cells for the Molecular Diagnosis of Rare Disorders. [PDF]

open access: yesInt J Mol Sci
Ludwig K   +6 more
europepmc   +1 more source

Clinical Phenotype Comparison in Polish Patient Cohorts with and Without Molecular Diagnosis of Dystonia. [PDF]

open access: yesJ Clin Med
Milanowski L   +10 more
europepmc   +1 more source

A Review of the Pathological and Molecular Diagnosis of Primary Myelofibrosis. [PDF]

open access: yesCancers (Basel)
Shao R   +8 more
europepmc   +1 more source

Molecular diagnosis.

open access: yesCanadian family physician Medecin de famille canadien, 2013
Recombinant DNA technology, one of the major controversial areas of biological research in the late 1970s, is now rapidly providing new avenues for diagnosis and treatment. With the early recognition that extensive DNA variation exists in human populations, molecular genetic diagnosis of a variety of common hereditary diseases has become a reality ...
openaire   +1 more source

Phenylalanine-tyrosine-catecholamine axis disorders: pathways, molecular diagnosis, therapeutics, and emerging translational monitoring technologies. [PDF]

open access: yesFront Mol Biosci
Armas Samaniego MI   +11 more
europepmc   +1 more source

Suidae Coronaviruses: Epidemiology, Transmission, and Molecular Diagnosis. [PDF]

open access: yesAnimals (Basel)
Ortello C   +6 more
europepmc   +1 more source

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