AmaGenesis kunye nama-chromosomes adluliselwa kumntwana

Ngoko, ngenxa yobuncwane, kukho iintambo kwi-molecule ye-DNA, ebizwa ngokuthi "iigleji." Ukudibanisa i-genes yomama noyise kwinqanaba lokujonga ibhiliyo kunokubhekwa njengoluvavanyo oluyimfuza. Leli yinkqubo yokuzalwa kobomi obutsha kwaye yanikela enye yeengcali ezikhokelayo kwimiba yokuziphatha kwe-genetics yaseMelika uRobert Robert Plomin. Kwi-biology, isakramente yokukhulelwa ingabhalwa ngendlela yefomula ethile, njengamajethi kunye nama-chromosomes adluliselwa kumntwana: iqanda ngalinye kunye ne-spermatozoon nganye inokudibanisa i-chromosomes ezingama-23. Ukudibanisa ngamabini, ngandlela-thile, i-chromosomes yomzali yenza ikhowudi ekhethekileyo yofuzo lomntu ozayo-i-genotype.

Nyaniso

Iintsana zifana nabafana. Uhlobo "lukhulelwe" kangangokuba loo mntu kwangoko wabona kumntwana ngokwakhe kunye nesimo saloo ntombi esakha ngokukhawuleza.


Umama okanye utata?

Umntwana, ngokomthetho, uzuze umbala wamehlo abo bazali, abavela kubo. Umzekelo, umama onamabala omdaka kunye noyise onamabala aluhlaza okomhlaza, nokuba umntwana uyinkopi kaPapa, amehlo aya kuba mnyama.

Ukuba omnye wabazali unentliziyo eboyiweyo, ngoko ke umntwana wokuqala, mhlawumbi, uya kuba neeralls.

Umntwana wokuqala ngumfana? Emva koko uya kuba njengomama ngoncedo lwe-gene kunye nama-chromosomes adluliselwe kumntwana. Intombazana ingenxa kabawo. Kwiimeko ezinjalo, bathi: "Kuya kuvuya."

Ingqondo kunye nobuchule belifa lifa kumama. Okukugqibela, ngendlela, kuqinisekiswa yenzululwazi. Inyaniso kukuba i-gene "ixanduva" ye-IQ i-X i-chromosomes, leyo ibhinqa inemibini (XX), kwaye amadoda analo (XY).

Uzalwe nguyise oqaqambileyo, intombazana inethuba elingcono lokubizwa ngokuba ngumfazi onobuqili, kodwa ngunyana womntu onobuchule, ubunjani bokuba "baphumle".

U-Svetlogolovym "kumama" umntwana uya kuba kuphela xa kwenzeka ukuba ii-blondes ziphakathi kunye nezihlobo zikayise.

Iimpawu ezinobungozi zikhokhwa kwiqondo lofuzo. Ukuxhomekeka kokunxiliswa kotywala kunqunywe yi-gene ejongene nokusetyenziswa kwe-enzyme eyenza utywala. Ukuba i-gene iguqulwa, ke umntwana wabantwana abathanda ukusela, unomdla wokusela utywala.


Umntu ngelifa

Inyaniso yokuba umlinganiso uzuzwa nge-gene kunye nama-chromosomes adluliselwe kumntwana akaqinisekanga ngokwesayensi. Nangona "i-gene aggression" efunyenwe yizinzulu kwiminyaka embalwa edlulileyo sele isinike umhlaba wokuthetha okunjalo. Enyanisweni, iimvavanyo ezisebenzayo ziye zazichasa. Kodwa ke, akusiyo into yokuba ama-rumors aseRashiya acebise, ekhetha umfazi wabo, ukujonga umkhwekazi. Zingaphi na izihlandlo sele usele utshilo, ukhangele intombi: "Ewe, unenkani - yonke inzala!" Okanye wambona kwindodana: "Oo, umlingiswa nguyise." Ewe, konke oku kunokubakho kwizinto ezibizwa ngokuba yiindleko zokukhuliswa. Inyaniso yokuba umntwana uyayikopisha kakuhle indlela abaziphatha ngayo yabazali, bebona indlela abaziphatha ngayo kwimo ethile. Emva koko uphinda isenzo kwiimeko ezifanayo. Okwangoku, izazinzulu ezisebenza ngokucacisa i-code ye-genetic code yomntu sele ziye zacaca ukuba ukuziphatha okuhloniphekileyo okanye ukuziphatha kakubi kubangama-34% ayenayo kithi. Bonke abanye bazimisele ngemfundo nakwimimandla. Kwaye kwanokukhethwa kobugcisa, sinama-40% enyanzelekile ukudibanisa ethile i-chromosomes. Ubuncinane, iimpawu zobunkokeli kwiimeko ezininzi zizuze ilifa. Mhlawumbi, yikho ke e-Russia kwakukho umgaqo-mandla wokudluliselwa kwamandla obukhosi - ukusuka kubaba ukuya kwonyana.


"Akukho mama, akukho ntata ..."

Enyanisweni, kwenzeka ukuba unyana okanye intombi ayikho njengabazali babo. Bakwazi ukuphinda ngokuphinda i-genotype yesinye isihlobo esikude. Okanye kude kakhulu. Kwaye ixesha elide sele lishiye kweli hlabathi.

Ukufana nomntu udla ngokukhathaza uyise kakhulu. Tshela umyeni wakho othandekayo ukuba umntwana wakho unjenge-grand-grand-mother-or-and-he will be calm for a while.

Kwaye kwakhona ubuyekeze iifoto zabantwana bakhe, kwaye uza kubona: ukubonakala komntwana omdala kutshintsha rhoqo kwaye emva konyaka okanye ezimbini iimvuthu zakho zingabonakalisa ezininzi iimpawu zakho.

I-Geneticist ne-Ph.D., uDean Heimer, wabonisa okokuqala ukuba "i-homosexual gene" ngo-1993, kwaye ngo-2004 wabhala incwadi malunga nokufumanisa "umthwalo wokholo kuThixo."

Oososayensi baseBrithani bahlalutya umlinganiso wama-paji angama-609 amawele kwaye kwathiwa ukuba ubuchule bokuqhuba ishishini lakho, ukuhlalisana kunye nokuqhelaniswa kwakukhethekileyo kumnye wabazalwana, ngoko bebekho ngokusemthethweni komnye. Nangona umkhwa onjengomnqweno wokuhlala ixesha elide phambi kweTV, i-45% ifa. Kwaye malunga "nomzimba we-genius" kunye nokuba kungenzeka ukuba yedwa, kunye nokufakelwa kwayo, izazinzulu ziye zahlala zixubusha ngokukodwa kwi-genotype yomntu othile. Kule meko, imbambano yembambano yinkalo yokuziphatha yenkxalabo, kwaye ingekho iingcamango zesayensi. Njengoko uSherlock Holmes wade wathi, ekujonge iipalraits zeBaskerville ubukhosi: "Ngoku ningakholelwa emva koku kokudlulela kwemiphefumlo!"


Umnyama, kunye nemigca

Ngekhulu le-19, i-telegonia yayithandwa. Ingcamango yokuba ukubonakala kweemvuthu ayiphenduliwanga ngohlobo lwezityalo zikayise, kodwa ngumlingani wokuqala womama. Kwavela emva kwecala kwihlabathi lamahashe.

Omnye umfuyi wagqiba ukuwela idibra enehashe. Wayengafuni ukuvelisa inzala kumntu ongaziwayo. Emva koko iintombi zaza zaza zityhulwa.