Add to ORKGBEALS' SYNDROME, ALSO KNOWN AS CONGENİTAL CONTRACTURAL ARACHNODACTYLY, IS A RECENT RECOGNİZED DİSORDER CHARACTERİZED BY MULTİPLE JOİNT CONTRACTURES
Laurence Moon-Bardet-Biedl syndrome is a rare autosomal recessive genetic disorder that mainly affec...
An infant girl with arachnodactyly and spontaneously resolving contractures who died in cardiac fail...
Weill–Marchesani syndrome is a rare connective tissue disorder, with a poorly understood etiology th...
Congenital contractural arachnodactyly (Beals syndrome) is an autosomal dominantly inherited connect...
Abstract Congenital contractural arachnodactyly (Beals syndrome) is an autosomal dominantly inherite...
We report the prenatal findings in two cases of Beals syndrome. Both pregnancies presented with clin...
Beals-Hecht syndrome or congenital contractural arachnodactyly (CCA) is a rare, autosomal dominant c...
Beals-Hecht syndrome or congenital contractural arachnodactyly (CCA) is a rare, autosomal dominant c...
A patient with typical congenital contractural arachnodactyly followed up from the age of 12 years t...
We report an Italian family suffering from chilblain. Seven members over three generations affected,...
We report on 2 unrelated Indian girls with blepharophimosis; arachnodactyly; digital contractures wh...
Congenital contractural arachnodactyly (CCA) is an autosomal dominant connective tissue disorder man...
Purpose Congenital contractural arachnodactyly (CCA) is an autosomal dominant connective tissue diso...
SummaryCongenital contractural arachnodactyly (CCA) is an autosomal dominant disorder that is phenot...
SYNOPSIS Two male cousins are reported with arachnodactyly, selective aminoaciduria, congenital cata...
Laurence Moon-Bardet-Biedl syndrome is a rare autosomal recessive genetic disorder that mainly affec...
An infant girl with arachnodactyly and spontaneously resolving contractures who died in cardiac fail...
Weill–Marchesani syndrome is a rare connective tissue disorder, with a poorly understood etiology th...
Congenital contractural arachnodactyly (Beals syndrome) is an autosomal dominantly inherited connect...
Abstract Congenital contractural arachnodactyly (Beals syndrome) is an autosomal dominantly inherite...
We report the prenatal findings in two cases of Beals syndrome. Both pregnancies presented with clin...
Beals-Hecht syndrome or congenital contractural arachnodactyly (CCA) is a rare, autosomal dominant c...
Beals-Hecht syndrome or congenital contractural arachnodactyly (CCA) is a rare, autosomal dominant c...
A patient with typical congenital contractural arachnodactyly followed up from the age of 12 years t...
We report an Italian family suffering from chilblain. Seven members over three generations affected,...
We report on 2 unrelated Indian girls with blepharophimosis; arachnodactyly; digital contractures wh...
Congenital contractural arachnodactyly (CCA) is an autosomal dominant connective tissue disorder man...
Purpose Congenital contractural arachnodactyly (CCA) is an autosomal dominant connective tissue diso...
SummaryCongenital contractural arachnodactyly (CCA) is an autosomal dominant disorder that is phenot...
SYNOPSIS Two male cousins are reported with arachnodactyly, selective aminoaciduria, congenital cata...
Laurence Moon-Bardet-Biedl syndrome is a rare autosomal recessive genetic disorder that mainly affec...
An infant girl with arachnodactyly and spontaneously resolving contractures who died in cardiac fail...
Weill–Marchesani syndrome is a rare connective tissue disorder, with a poorly understood etiology th...