x linked

It is usually inherited as an autosomal dominant trait, although autosomal recessive and X-linked inheritance are seen less commonly.

Medically, the condition is called X-linked Severe Combined Immunodeficiency (X-SCID).

Androgen insensitivity is an X-linked disorder of male sexual differentiation resulting from a defective androgen receptor.

Testicular feminization syndrome, the most common type of male pseudohermaphroditism, is an X-linked recessive disorder.

As an X-linked condition, choroideremia usually affects men, leading to severe vision loss or blindness in middle age.

ABSTRACT: Objective To identify the mutations of ED1 gene in a family with X-linked hypohidrotic ectodermal dysplasia.

The molecular diagnosis for X-linked adrenoleukodystrophy (ALD) using mutational analysis at genomic DNA level is important.

However, baldness is another X-linked recessive trait; you inherit it from your mother.

This is an X-linked deficiency of one of the enzymes in the urea cycle.

Her team focused on a particular protein involved in the NF-kappa B pathway called the "X-linked inhibitor of apoptosis" (XIAP).

Here we describe a previously unreported X-linked brain malformation syndrome caused by mutations of CASK.

Investigation in 308 family trios suggested a co-dominant X-linked inheritance and mutations were not found.

Sex-limited --- A trait that is expressed in only one sex, although the gene that determines the trait is not X-linked.

bilateral sensorineural hearing loss, which is never congenital in onset, occurs in 90% of hemizygous males with X-linked AS.

It can be autosomal dominant, autosomal recessive, or X-linked mode of inheritance.

A characteristic of X-linked inheritance is that fathers cannot pass X-linked traits to their sons .

Clinical study of a single congenital stapes malformation with possible X-linked dominant inheritance

A retrospective study of one case of X-linked agammaglobulinemia

Expression and Significance of X-linked Inhibitor of Apoptosis Protein and Its Antagonized Proteins in Acute Leukemia

Prokaryotic Expression and Characterization of ATP-binding Domain of X-linked Adrenoleukodystrophy Protein

Investigation of steroid sulfatase gene in two pedigrees with X-linked ichthyosis

Genetical Diagnosis in A Family with X-linked Hypohidrotic Ectodermal Dysplasia

Mutation analysis of dystrophin gene and clinical evaluation of phenotypes in X-linked dilated cardiomyopathy

X-linked inhibitor of apoptosis protein and its clinic significance in leukemia

Juvenile idiopathic arthritis in patients with X-linked agammaglobulinemia

Prenatal diagnosis of X-linked anhidrotic ectodermal dysplasia with X-chromosome inversion

Inhibition of ovarian cancer growth by small interfering RNA targeting X-linked inhibitor of apoptosis gene

X-linked inhibitor of apoptosis protein is regulated by laminar shear stress in cultured endothelial cells

Positional cloning in Chinese X-linked congenital inner ear malformation family

Investigation of STS Gene in a Pedigree with X-Linked Ichthyosis

Roles of X-Linked Inhibitor of Apoptosis Protein in Ovarian Epithelial Cancer Cell Line

A novel RPGR gene mutation in a Chinese family with X-linked dominant retinitis pigmentosa

Preliminary study on chromosome location of X-linked high myopia

A typical X-linked inheritance pedigree