Pages that link to "Immunoglobulin superfamily"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to Immunoglobulin superfamily:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Tumor necrosis factor (← links | edit)
- Osteopetrosis (← links | edit)
- Donohue syndrome (← links | edit)
- Aldesleukin (← links | edit)
- Interleukin-2 (← links | edit)
- Glanzmann thrombasthenia (← links | edit)
- Laron syndrome (← links | edit)
- Thanatophoric dysplasia (← links | edit)
- Waardenburg syndrome (← links | edit)
- Alpha Interferon (← links | edit)
- Interferon Beta (← links | edit)
- Nevoid basal cell carcinoma syndrome (← links | edit)
- Peginterferon alfa-2b (← links | edit)
- PEG-Intron (← links | edit)
- Recombinant interferon alfa-2b (← links | edit)
- Anti-c-fms monoclonal antibody AMG 820 (← links | edit)
- Familial hypercholesterolemia (← links | edit)
- Selective IgA deficiency (← links | edit)
- Interferon type II (← links | edit)
- Interferon type I (← links | edit)
- Gonadotropin-releasing hormone insensitivity (← links | edit)
- Gonadotropin insensitivity (← links | edit)
- Dictionary-of-medicine-I (← links | edit)
- Antley–Bixler syndrome (← links | edit)
- Cenani–Lenz syndactylism (← links | edit)
- Follicle-stimulating hormone insensitivity (← links | edit)
- Leukocyte adhesion deficiency-1 (← links | edit)
- Loeys–Dietz syndrome (← links | edit)
- TNF receptor associated periodic syndrome (← links | edit)
- WHIM syndrome (← links | edit)
- Worth syndrome (← links | edit)
- Encyclopedia of medicine (← links | edit)
- Bone morphogenetic proteins (← links | edit)
- X-linked severe combined immunodeficiency (← links | edit)
- Kallmann syndrome (← links | edit)
- Hereditary hemorrhagic telangiectasia (← links | edit)
- Familial exudative vitreoretinopathy (← links | edit)
- Common variable immunodeficiency (← links | edit)
- Crouzon syndrome (← links | edit)
- Congenital amegakaryocytic thrombocytopenia (← links | edit)
- Congenital insensitivity to pain with anhidrosis (← links | edit)
- Apert syndrome (← links | edit)
- Gastrointestinal Stromal Tumors (← links | edit)
- Tumor necrosis factor receptor-associated periodic syndrome (← links | edit)
- Nephrogenic diabetes insipidus (← links | edit)
- XX gonadal dysgenesis (← links | edit)
- Worth type autosomal dominant osteosclerosis (← links | edit)
- Juvenile polyposis syndrome (← links | edit)
- Familial hypocalciuric hypercalcemia type 1 (← links | edit)
- Familial hypocalciuric hypercalcemia type 3 (← links | edit)