To access publisher full text version of this article. Please click on the hyperlink in Additional Links fieldAutosomal recessive macular corneal dystrophy (MCD) is a heterogeneous disorder leading to visual impairment. Sixteen American and Icelandic families (11 type I and 5 type II) were analyzed for linkage, by use of 208 polymorphic microsatellite markers. A significant maximum LOD score Zmax of 7.82 at a maximum recombination fraction (thetamax) of .06 was found with the 16q22 locus D16S518 for MCD type I. In addition, a peak LOD score of 2.50 at a recombination fraction of .00 was obtained for the MCD type II families, by use of the identical marker. These findings raise the possibility that MCD type II may be due to the same genetic ...
Purpose To describe a German family with clinical and genetic evidence of autosomal dominant North ...
Purpose. Macular corneal dystrophy (MCD) is a rare autosomal recessive disorder that is characterize...
Autosomal dominant North Carolina macular dystrophy (NCMD) or central areolar pigment epithelial dys...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
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Background and objective: North Carolina macular dystrophy (NCMD) is a very rare autosomal dominant ...
AbstractNorth Carolina macular dystrophy (NCMD) is an autosomal dominant macular disease, was mapped...
BACKGROUND: Developmental macular disorders are a heterogeneous group of rare retinal conditions tha...
PURPOSE: To describe the clinical findings and to identify the genetic locus in a Dutch family with ...
<p><i>Background</i>: Developmental macular disorders are a heterogeneous group of rare retinal cond...
Macular corneal dystrophy (MCD) is an autosomal recessive disease characterized by corneal opacities...
Macular Telangiectasia type 2 (MacTel) is a relatively rare macular disease of adult onset presentin...
Schnyder's crystalline corneal dystrophy (SCCD) is a rare autosomal dominant eye disease with a spec...
Macular Telangiectasia type 2 (MacTel) is a relatively rare macular disease of adult onset presentin...
Purpose To describe a German family with clinical and genetic evidence of autosomal dominant North ...
Purpose. Macular corneal dystrophy (MCD) is a rare autosomal recessive disorder that is characterize...
Autosomal dominant North Carolina macular dystrophy (NCMD) or central areolar pigment epithelial dys...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
To access publisher full text version of this article. Please click on the hyperlink in Additional L...
Background and objective: North Carolina macular dystrophy (NCMD) is a very rare autosomal dominant ...
AbstractNorth Carolina macular dystrophy (NCMD) is an autosomal dominant macular disease, was mapped...
BACKGROUND: Developmental macular disorders are a heterogeneous group of rare retinal conditions tha...
PURPOSE: To describe the clinical findings and to identify the genetic locus in a Dutch family with ...
<p><i>Background</i>: Developmental macular disorders are a heterogeneous group of rare retinal cond...
Macular corneal dystrophy (MCD) is an autosomal recessive disease characterized by corneal opacities...
Macular Telangiectasia type 2 (MacTel) is a relatively rare macular disease of adult onset presentin...
Schnyder's crystalline corneal dystrophy (SCCD) is a rare autosomal dominant eye disease with a spec...
Macular Telangiectasia type 2 (MacTel) is a relatively rare macular disease of adult onset presentin...
Purpose To describe a German family with clinical and genetic evidence of autosomal dominant North ...
Purpose. Macular corneal dystrophy (MCD) is a rare autosomal recessive disorder that is characterize...
Autosomal dominant North Carolina macular dystrophy (NCMD) or central areolar pigment epithelial dys...