However, evidence of autosomal recessive inheritance has also been reported.

Some cases appear to follow an autosomal recessive inheritance pattern.

In extremely rare cases, autosomal recessive inheritance has been reported.

Both autosomal dominant and recessive inheritance have been reported in the medical literature.

Recessive inheritance is when both matching genes must be abnormal to cause disease.

This form of genetic transmission is called autosomal recessive inheritance.

This locus was discovered, however, using an autosomal recessive inheritance model.

This family demonstrates the autosomal recessive inheritance of the disorder.

However, in some cases, family histories suggest autosomal dominant or recessive inheritance.

The disorder is inherited with an X-linked recessive inheritance pattern.

Although the reason for this difference in risk is unknown, possible hypotheses include X-linked or recessive inheritance.

He described the nature of recessive inheritance of most enzyme defects.

In most cases these mutations are the result of an autosomal recessive inheritance pattern.

Autosomal recessive inheritance means two copies of the gene in each cell are altered.

The different clinical presentations are complicated by the pattern of X-linked recessive inheritance.

Zunich-Kay syndrome is considered to have an autosomal recessive inheritance pattern.

Most cases are inherited as one or another of two types of autosomal recessive inheritance.

Diseases of X-linked recessive inheritance, such as colour blindness, occur more frequently in men.

The first group, termed nephronophthisis, is characterized by an autosomal recessive inheritance.

X-linked autosomal recessive inheritance has not been ruled out.

It is a genetic disorder that typically follows an autosomal recessive inheritance pattern.

In addition, a segregation analysis of 1,546 families from Finland found evidence for Mendelian recessive inheritance.

Most cases of Fanconi anemia have autosomal recessive inheritance.

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.