Marfan syndrome (MFS) (MIM 154700) is a heritable disorder of connective tissue characterised by excessive height and limb length disproportion, together with ocular, cardiovascular and skeletal manifestations. The condition is an autosomal dominant trait, and can be transmitted from generation to generation with variable severity. The determinant gene FBN1 is situated at the chromosomal locus 15q21.1 and codes for the protein fibrillin-1
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is an autosomal dominant disorder of the connective tissue due to mutations of...
Abstract Background and Aims Marfan syndrome (MFS) is an autosomal dominant genetic disorder caused ...
Genetic testing is aiding rapid diagnosis of Marfan syndrome as a basis for management of eye, heart...
Introduction: Marfan syndrome (SM) is a systemic disorder caused by mutations in the extracellular m...
Background: Marfan syndrome (MFS) is an underrecognized heritable connective tissue disorder resulti...
Background: Marfan syndrome (MFS) is an underrecognized heritable connective tissue disorder resulti...
In order to estimate the contribution of mutations at the fibrillin,1 locus (FBN1) to classical Marf...
Purpose: To describe a novel mutation in the fibrillin-1 (FBN1) gene in a large Pakistani family wit...
Marfan syndrome (MFS) is an inherited connective tissue disorder caused by heterozygous mutations in...
Abstract Background The genetic approach to Marfan syndrome (MFS) ha...
PURPOSE: To describe a novel mutation in the fibrillin-1 (FBN1) gene in a large Pakistani family wit...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is an autosomal dominant disorder of the connective tissue due to mutations of...
Abstract Background and Aims Marfan syndrome (MFS) is an autosomal dominant genetic disorder caused ...
Genetic testing is aiding rapid diagnosis of Marfan syndrome as a basis for management of eye, heart...
Introduction: Marfan syndrome (SM) is a systemic disorder caused by mutations in the extracellular m...
Background: Marfan syndrome (MFS) is an underrecognized heritable connective tissue disorder resulti...
Background: Marfan syndrome (MFS) is an underrecognized heritable connective tissue disorder resulti...
In order to estimate the contribution of mutations at the fibrillin,1 locus (FBN1) to classical Marf...
Purpose: To describe a novel mutation in the fibrillin-1 (FBN1) gene in a large Pakistani family wit...
Marfan syndrome (MFS) is an inherited connective tissue disorder caused by heterozygous mutations in...
Abstract Background The genetic approach to Marfan syndrome (MFS) ha...
PURPOSE: To describe a novel mutation in the fibrillin-1 (FBN1) gene in a large Pakistani family wit...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is a chronic, life-threatening, autosomal dominant connective tissue disorder ...
Marfan Syndrome (MFS) is an autosomal dominant disorder of the connective tissue due to mutations of...