W. Wertelecki

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.

Colige, A, Sieron, A L, Li, S W, Schwarze, U, Petty, E, Wertelecki, W, ...

Ehlers-Danlos syndrome (EDS) type VIIC is a recessively inherited connective-tissue disorder, characterized by extreme skin fragility, characteristic facies, joint laxity, droopy skin, umbilical...

Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen.

Smith, L T, Wertelecki, W, Milstone, L M, Petty, E M, Seashore, M R, Braverman, I M, ...

Dermatosparaxis is a recessively inherited connective-tissue disorder that results from lack of the activity of type I procollagen N-proteinase, the enzyme that removes the amino-terminal propeptides...

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Rouleau, G A, Seizinger, B R, Wertelecki, W, Haines, J L, Superneau, D W, Martuza, R L, ...

Neurofibromatosis 2 or bilateral acoustic neurofibromatosis (NF2) is a severe autosomal dominant disorder characterized by the development of multiple tumors of the nervous system, including...

Human Ehlers-Danlos syndrome type VII C and bovine dermatosparaxis are caused by mutations in the procollagen I N-proteinase gene.

Colige, A, Sieron, A L, Li, S W, Schwarze, U, Petty, E, Wertelecki, W, ...

Ehlers-Danlos syndrome (EDS) type VIIC is a recessively inherited connective-tissue disorder, characterized by extreme skin fragility, characteristic facies, joint laxity, droopy skin, umbilical...

Human dermatosparaxis: a form of Ehlers-Danlos syndrome that results from failure to remove the amino-terminal propeptide of type I procollagen.

Smith, L T, Wertelecki, W, Milstone, L M, Petty, E M, Seashore, M R, Braverman, I M, ...

Dermatosparaxis is a recessively inherited connective-tissue disorder that results from lack of the activity of type I procollagen N-proteinase, the enzyme that removes the amino-terminal propeptides...

Flanking markers bracket the neurofibromatosis type 2 (NF2) gene on chromosome 22.

Rouleau, G A, Seizinger, B R, Wertelecki, W, Haines, J L, Superneau, D W, Martuza, R L, ...

Neurofibromatosis 2 or bilateral acoustic neurofibromatosis (NF2) is a severe autosomal dominant disorder characterized by the development of multiple tumors of the nervous system, including...