లేదా ఒక Autosom సంబంధించిన,

Adjective:

ఆటోసోమల్,

autosomal తెలుగు అర్థానికి ఉదాహరణ:

α-, β- తలసేమియా అప్రభావితమైన ఆటోసోమల్ (autosomal) పద్దతిలో వారసత్వముగా వ్యాపిస్తాయి.

బిడ్డకు అప్రభావితమైన ఆటోసోమల్ (autosomal) వంటి వ్యాధులకు తల్లితండ్రులిద్దరు కారకులవుతారు.

నిదర్శనాల ప్రకారం అప్రభావితమైన ఆటోసోమల్ (autosomal) పద్దతిలో వారసత్వముగా వ్యాపించిన α-, β- తలసేమియా అధికముగా నమోదయ్యాయి.

ఆటోసోమల్ DNA ఆధారాలన్నీ కూడా ప్రధానంగా ఇటీవలి ఆఫ్రికన్ మూలానికే మద్దతు ఇచ్చాయి.

ఆటోసోమల్ మైక్రోసాటిలైట్ మార్కర్లను హువా లియు తదితరులు విశ్లేషించి అవి 56,000 సంవత్సరాల క్రితం నాటివని తేల్చారు.

autosomal's Usage Examples:

is a common, autosomal-dominant, genetic condition of the skin"s hair follicles characterized by the appearance of possibly itchy, small, gooseflesh-like.

an autosomal recessive congenital immunodeficiency condition due to underdevelopment of the thymus.

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

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

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

It is an autosomal recessive, multiple malformation syndrome caused by a mutation in the enzyme 7-Dehydrocholesterol reductase encoded by the DHCR7 gene.

Thiamine responsive megaloblastic anemia syndrome (also known as Rogers Syndrome) is a very rare autosomal recessive genetic disorder affecting a thiamine.

Char syndrome is an autosomal dominant congenital disease caused by mutations in TFAP2B gene which affects the development of the bones of the face as.

Hartnup disease (also known as "pellagra-like dermatosis" and "Hartnup disorder") is an autosomal recessive metabolic disorder affecting the absorption.

called osteosclerotic bone dysplasia, is a rare autosomal recessive congenital disorder characterized by craniofacial anomalies including microcephaly, noticeably.

Trichothiodystrophy (TTD) is an autosomal recessive inherited disorder characterised by brittle hair and intellectual impairment.

recessive polycystic kidney disease (ARPKD) is primarily diagnosed in infants and young children while autosomal dominant polycystic kidney disease (ADPKD).

[citation needed] The term PPS has also been used for two rare autosomal recessively inherited conditions: Lethal PPS and PPS with Ectodermal Dysplasia.