Noun:

सुप्त जनुक,

recessive gene's Usage Examples:

Lethal congenital contracture syndrome 1 (LCCS1), also called Multiple contracture syndrome, Finnish type, is an autosomal recessive genetic disorder characterized.

Primary ciliary dyskinesia (PCD), is a rare, ciliopathic, autosomal recessive genetic disorder that causes defects in the action of cilia lining the respiratory.

sepal-like organs, originating via a mutation governed by a single recessive gene.

shock, the non-Ginger parents of the Ginger kids, who each carry a recessive gene that has caused them to have Ginger kids, possess the same prejudice.

partial or total alopecia of the head and limbs; this is caused by a recessive gene.

Chestnut is produced by a recessive gene.

recessive genes including: The "Red cheek" Bagot - which sports red/gold "blusher" on the cheeks but not through the coat.

autosomal recessive genetic disorder that causes defects in the action of cilia lining the respiratory tract (lower and upper, sinuses, Eustachian tube.

keratoderma with periodontitis, is an autosomal recessive genetic disorder caused by a deficiency in cathepsin C.

– dominant gene – recessive gene genetic interactions – Mendel"s law of segregation – genetic mosaic – maternal effect – penetrance – complementation.

inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen).

The distinctive color is caused by the action of an autosomal recessive gene, commonly designated as "lav", which reduces the expression of eumelanin.

them with only rods, a recessive genetic disorder that causes total color blindness in sufferers.

Synonyms:

factor, gene, cistron,

Antonyms:

exon, intron,