Pages that link to "Pelger–Huët anomaly"
From WikiMD's Wellness Encyclopedia
The following pages link to Pelger–Huët anomaly:
Displaying 6 items.
- Miscellaneous (← links | edit)
- Dictionary of hematology (← links | edit)
- Ovoid neutrophil nuclei, developmental delay, epilepsy and skeletal abnormalities (redirect page) (← links | edit)
- Pelger Huet anomaly (redirect page) (← links | edit)
- Pelger-Huet nuclear anomaly (redirect page) (← links | edit)
- Pelger–Huet anomaly (redirect page) (← links | edit)
- Laminopathy (← links | edit)
- Hereditary spherocytosis (← links | edit)
- Sepsis (← links | edit)
- Complete blood count (← links | edit)
- Dilated cardiomyopathy (← links | edit)
- Hereditary elliptocytosis (← links | edit)
- Hypertrophic cardiomyopathy (← links | edit)
- Alexander disease (← links | edit)
- Reticular pigmented anomaly of the flexures (← links | edit)
- May–Hegglin anomaly (← links | edit)
- Boomerang dysplasia (← links | edit)
- Marfan syndrome (← links | edit)
- Familial adenomatous polyposis (← links | edit)
- Epidermolysis bullosa simplex (← links | edit)
- Wiskott Aldrich syndrome (← links | edit)
- Hemochromatosis - Not a rare disease (← links | edit)
- MYH9 related thrombocytopenia (← links | edit)
- Azotemia (← links | edit)
- Buschke–Ollendorff syndrome (← links | edit)
- Arrhythmogenic cardiomyopathy (← links | edit)
- Asphyxiating thoracic dysplasia (← links | edit)
- Charcot–Marie–Tooth disease (← links | edit)
- Emery–Dreifuss muscular dystrophy (← links | edit)
- Weill–Marchesani syndrome (← links | edit)
- Neutrophil-specific granule deficiency (← links | edit)
- Pelger–Huët anomaly (← links | edit)
- Naxos syndrome (← links | edit)
- Usher syndrome, type 1 (← links | edit)
- Usher syndrome type 2A (← links | edit)
- Familial partial lipodystrophy type 2 (← links | edit)
- Limb-girdle muscular dystrophy type 2I (← links | edit)
- Limb-girdle muscular dystrophy, type 2C (← links | edit)
- Epidermolysa bullosa simplex with muscular dystrophy (← links | edit)
- Limb-girdle muscular dystrophy type 2A (← links | edit)
- Limb-girdle muscular dystrophy type 2B (← links | edit)
- Intermediate congenital nemaline myopathy (← links | edit)
- Epidermolysis bullosa simplex, Dowling-Meara type (← links | edit)
- Epidermolysis bullosa simplex, generalized (← links | edit)
- Epidermolysis bullosa simplex, localized (← links | edit)
- Epidermolysis bullosa, lethal acantholytic (← links | edit)
- Hematology/oncology (← links | edit)
- Auer rod (← links | edit)
- Template:Cytoskeletal defects (← links | edit)
- Template:Abnormal clinical and laboratory findings for blood (← links | edit)
