Discover open access scientific publications

Search, annotate, share and cite publications

Publications by M. Menegatti

Phenotype and Genotype Report on Homozygous and Heterozygous Patients With Congenital Factor X Deficiency

English

Related publications

Circumcision in Patients With Congenital Factor X Deficiency

Indian Journal of Pediatrics

English

AB110. Genotype and Phenotype of 107 Patients With Congenital Hyperinsulinism

Annals of Translational Medicine

English

Congenital Factor X Deficiency in Japan.

Tohoku Journal of Experimental Medicine

Molecular Biology

English

Genotype-Phenotype Correlation in 1,507 Families With Congenital Adrenal Hyperplasia Owing to 21-Hydroxylase Deficiency

Proceedings of the National Academy of Sciences of the United States of America

Multidisciplinary

English

Phenotype in Homozygous and Heterozygous Carriers of BEST1 Mutations in Autosomal Recessive Bestrophinopathy

Acta Ophthalmologica

English

Familial Association of Hypoplasminogenemia and Heterozygous Factor v Deficiency

Clinical and Applied Thrombosis/Hemostasis

English

Heterozygous Glucokinase Splicing Mutation - Identical Genotype With Variable Phenotype in a Single Family

Endocrine Abstracts

English

Variability of Clinical Manifestation of Factor VII-deficiency in Homozygous and Heterozygous Subjects of the European F7 Gene Mutation A294V

English

Severe Congenital Deficiency of Factor XIII: A Brief Report of Morbidity and Mortality Rates of Severe Congenital Deficiency of Factor 13 in Iran

Iranian South Medical Journal

English