Dodatkowe przykłady dopasowywane są do haseł w zautomatyzowany sposób - nie gwarantujemy ich poprawności.
This locus was discovered using an autosomal recessive inheritance model.
Autosomal recessive inheritance has been suggested in some cases.
Zunich-Kay syndrome is considered to have an autosomal recessive inheritance pattern.
Autosomal recessive inheritance means two copies of the gene in each cell are altered.
Like the maternal molecules that need to be normal, many of these are also a inherited with autosomal recessive inheritance.
It is a genetic disorder that typically follows an autosomal recessive inheritance pattern.
Since many of these conditions have an autosomal recessive inheritance pattern, they are rare and can be associated with consanguinity.
It exhibits autosomal recessive inheritance, and the responsible gene is located at chromosome 20q13.
Usher syndrome is passed to succeeding family generations through the autosomal recessive inheritance pattern.
The mutation has an autosomal recessive inheritance pattern.
The pedigrees are consistent with autosomal recessive inheritance.
Many affected individuals are within the same family, and pedigree data supports that the disease is acquired through autosomal recessive inheritance.
All four types have autosomal recessive inheritance.
Production of correct proteins from the great majority of these genes is likely to depend on autosomal recessive inheritance.
Autosomal recessive inheritance patterns of RP have been identified in at least 45 genes.
Evidence for autosomal recessive inheritance comes from three Amish sibships whose parents all shared a common ancestor.
In autosomal recessive inheritance, two copies of an abnormal gene must be present in order for the disease to develop.
It is of autosomal recessive inheritance.
Metachromatic leukodystrophy, like most enzyme deficiencies, has an autosomal recessive inheritance pattern.
Autosomal Recessive Inheritance is another group.
Autosomal recessive inheritance, where both copies of a gene contain mutations, is especially associated with C5-C6 fusion.
Sebaceous Adenitis is an autoimmune skin disorder believed to be of autosomal recessive inheritance.
Both autosomal dominant and autosomal recessive inheritance have been reported with this disorder as has an acquired form of the disease.
EDS dermatosparaxis type has autosomal recessive inheritance.
Osteopetrosis can be inherited in two ways, termed autosomal recessive inheritance and autosomal dominant.