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Analyse hematological test results
Automated analysers in the medical laboratory
Automatic analysers
Describe hematological test results
Diagnosis and treatment of blood diseases
European Society of Hematology
General haematology
General hematology
Hemato-oncology
Hematology Report
Hematology analysers
Hematology-oncology
ISH
International Society of Hematology
Interpret hematological investigations
Interpret hematological test results
Medical laboratory instruments
Onco-hematology
Oncohematology
Scientific Products Diff-Trol SMX hematology control

Traduction de «Hematology Report » (Anglais → Français) :

Hematology Report [ Patient's Demographics - National Defence Medical Centre ]

Rapport d'hématologie [ Démographiques du patient - Centre médical - Défense nationale ]


describe hematological test results | interpret hematological investigations | analyse hematological test results | interpret hematological test results

interpréter des résultats de tests hématologiques


A rare genetic hematologic disorder characterized by progressive trilineage bone marrow failure (with hypocellularity), developmental delay with learning disabilities and microcephaly. Mild facial dysmorphism and hypotonia have also been reported. Th

syndrome de pancytopénie-retard de développement


International Society of Hematology [ ISH | European Society of Hematology ]

Société internationale d'hématologie [ SIH | Société européenne d'hématologie ]


S/P Diff-Trol SMX hematology control [ Scientific Products Diff-Trol SMX hematology control ]

solution de contrôle Diff-Trol SMX pour hématologie de Scientific Products


hematology-oncology | hemato-oncology | oncohematology | onco-hematology

hématologie-oncologie | hémato-oncologie | oncohématologie | onco-hématologie


diagnosis and treatment of blood diseases | general haematology | general hematology

hématologie générale


automatic analysers | medical laboratory instruments | automated analysers in the medical laboratory | hematology analysers

analyseurs de laboratoire automatiques


Pyknoachondrogenesis is a lethal skeletal osteochondrodysplasia characterised by severe generalised osteosclerosis. The disease is very rare and only five cases (four males and one female) have been reported in the literature so far. Pyknoachondrogen

pycnoachondrogénèse


An extremely rare tumour association characterised by dual predisposition to melanoma and neural system tumours (typically astrocytoma). Fewer than 20 affected families have been reported to date. Affected individuals had cutaneous melanoma in associ

syndrome mélanome-tumeur du système nerveux


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