বা একটি autosome সংক্রান্ত

autosomal's Usage Examples:

The terms autosomal dominant or autosomal recessive are used to describe gene variants on non-sex chromosomes.

who are carriers of a faulty gene (autosomal recessive inheritance) or from a parent with the disorder (autosomal dominant inheritance).

Autosomal genetic disorders which exhibit Mendelian inheritance can be inherited either in an autosomal dominant or recessive fashion.

follows general inheritance rules and can be inherited in an autosomal dominant, autosomal recessive or X-linked recessive manner.

, dominant, recessive, autosomal or X-linked).

It is autosomal dominant, meaning that only one affected chromosome is needed for the.

sometimes characterised as "autosomal trisomies" (trisomies of the non-sex chromosomes) and "sex-chromosome trisomies.

CADASIL or CADASIL syndrome, involving cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, is the most common.

extra autosomal chromosomes among live births are 21, 18 and 13.

RLBP1 (autosomal recessive, Bothnia type RP) RP1 (autosomal dominant, RP1) RHO (autosomal dominant, RP4) RDS (autosomal dominant, RP7) PRPF8 (autosomal dominant.

having their own pathology and genetic cause: autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD).

for different types of genealogical research: autosomal (atDNA), mitochondrial (mtDNA), and Y-DNA.

Monilethrix (also referred to as beaded hair) is a rare autosomal dominant hair disease that results in short, fragile, broken hair that appears beaded.

Examples of autosomal dominant traits and disorders are Huntington's disease and achondroplasia.

DFNA: nonsyndromic deafness, autosomal dominant DFNB: nonsyndromic deafness, autosomal recessive DFNX: nonsyndromic deafness, X-linked.

caused by a genetic mutation in the IGHMBP2 gene and is inherited in an autosomal recessive manner.

can be inherited in an autosomal dominant, autosomal recessive, or X-linked manner.

[citation needed] Many types of autosomal dominant cerebellar ataxias.

Muscular dystrophies may be X-linked recessive, autosomal recessive, or autosomal dominant.

Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull,.

autosomal's Meaning':

of or relating to an autosome