dominant inheritance

They were mostly thought to have autosomal dominant inheritance patterns.

However, some cases reported in the medical literature suggest an autosomal dominant inheritance pattern.

However, autosomal dominant inheritance has not been ruled out.

It is a genetic disorder with an autosomal dominant inheritance pattern.

Autosomal Dominant inheritance shows a later onset and slower progression.

It may appear either sporadically or exhibit autosomal dominant inheritance.

The deficiency is transmitted through an autosomal dominant inheritance pattern.

With "autosomal dominant inheritance," men and women are equally likely to inherit the disease.

In other instances, the disorder is familial with autosomal dominant inheritance.

They were found in heterozygotes, suggesting an autosomal dominant inheritance pattern.

Cancers occurring in multiple generations of a family (autosomal dominant inheritance).

Evidence indicates that the condition is sometimes familial, suggesting autosomal dominant inheritance.

Genetic factors: an autosomal dominant inheritance pattern has been postulated.

Approximately 10-15 percent of cases of this syndrome run in families and show autosomal dominant inheritance.

It is transmitted by autosomal dominant inheritance (simple dominance).

In most cases, Trichorhinophalangeal syndrome type I has autosomal dominant inheritance.

These tumors tend to involve the entire extent of the nerve and show a strong autosomal dominant inheritance.

Most currently known cancer susceptibility syndromes follow an autosomal dominant inheritance pattern.

This suggests an autosomal dominant inheritance but additional cases need to be investigated to establish this.

Familial cases are associated with autosomal dominant inheritance.

An autosomal dominant inheritance with age dependency and variable penetrance has been reported, although not all studies support this theory.

The disorder can be acquired or inherited, the hereditary form having an autosomal dominant inheritance pattern.

Autosomal dominant inheritance means one copy of the altered gene in each cell is sufficient to cause the disorder.

Rarely, this condition may be the result of de novo mutations, or an autosomal dominant inheritance pattern.

X-linked dominant inheritance will show the same phenotype as a heterozygote and homozygote.