Congenital deficiency of C2 and factor B.

A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes).

[Factor V congenital deficiency: about a case].

Liver transplant for congenital factor VII deficiency.

Congenital factor XIII deficiency in a neonate.

Deficiency in complement factor B.

Recurrent thrombophlebitis and pulmonary emboli in congenital factor 5 deficiency.

Genetic Confirmation of Congenital Factor V Deficiency in Korean Patients.

Congenital factor VII deficiency. A report of four new cases.

Limited proteolysis of complement components C2 and factor B. Structural analogy and limited sequence homology.

Transcriptional termination between the closely linked human complement genes C2 and factor B: common termination factor for C2 and c-myc?

Hereditary complement (C2) deficiency with dermatomyositis.

A case of congenital factor V deficiency combined with multiple congenital anomalies: successful management of palatoplasty.

Circumcision in patients with congenital factor X deficiency.

Defective yeast opsonization and C2 deficiency in atopic patients.

Patients with congenital factor V deficiency have decreased factor Xa binding sites on their platelets.

Congenital CD59 Deficiency.

Congenital limb deficiency disorders.

Congenital combined deficiency of factor V and factor VIII with acquired ichthyosis, epidermodysplasia verruciformis, and immunological abnormalities.

Hereditary C2 deficiency associated with common variable immunodeficiency.

Congenital deficiency of alpha-fetoprotein.

Factor v deficiency associated with congenital cardiac disorder and intracranial hemorrage.

Complement C3, C2, and factor B gene polymorphisms and age-related macular degeneration in a Greek cohort study.

Congenital adrenal hypoplasia and gonadotrophin deficiency.

Congenital diaphragmatic hernia and iron deficiency anemia.

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A restriction fragment of the C2 gene is a unique marker for C2 deficiency and the uncommon C2 allele C2*B (a marker for type 1 diabetes).

[Factor V congenital deficiency: about a case].

Liver transplant for congenital factor VII deficiency.

Congenital factor XIII deficiency in a neonate.

Deficiency in complement factor B.

Recurrent thrombophlebitis and pulmonary emboli in congenital factor 5 deficiency.

Genetic Confirmation of Congenital Factor V Deficiency in Korean Patients.

Congenital factor VII deficiency. A report of four new cases.

Limited proteolysis of complement components C2 and factor B. Structural analogy and limited sequence homology.

Transcriptional termination between the closely linked human complement genes C2 and factor B: common termination factor for C2 and c-myc?

Hereditary complement (C2) deficiency with dermatomyositis.

A case of congenital factor V deficiency combined with multiple congenital anomalies: successful management of palatoplasty.

Circumcision in patients with congenital factor X deficiency.

Defective yeast opsonization and C2 deficiency in atopic patients.

Patients with congenital factor V deficiency have decreased factor Xa binding sites on their platelets.

Congenital CD59 Deficiency.

Congenital limb deficiency disorders.

Congenital combined deficiency of factor V and factor VIII with acquired ichthyosis, epidermodysplasia verruciformis, and immunological abnormalities.

Hereditary C2 deficiency associated with common variable immunodeficiency.

Congenital deficiency of alpha-fetoprotein.

Factor v deficiency associated with congenital cardiac disorder and intracranial hemorrage.

Complement C3, C2, and factor B gene polymorphisms and age-related macular degeneration in a Greek cohort study.

Congenital adrenal hypoplasia and gonadotrophin deficiency.

Congenital diaphragmatic hernia and iron deficiency anemia.

Congenital deficiency of C2 and factor B.

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