Results 111 to 120 of about 40,187 (197)

Multiple copy number variation in a patient with Kleefstra syndrome. [PDF]

open access: yesRev Paul Pediatr, 2023
Lee TN   +6 more
europepmc   +1 more source

Genetika és egészség

open access: yes, 2016
Hogyan szabalyozza taplalkozasunk a genkifejeződest es a betegseghajlamot? Mik az őssejtek, es mire hasznalhatjuk őket a gyogyitasban? Hogy valtoztatja meg a bennunk elő mikrovilag a betegseghajlamunkat? Mi a halozati medicina, es mi a jelentősege a gyogyszerfejlesztesben?
openaire   +1 more source

OPTIMASI PUSAT CLUSTER K-PROTOTYPE DENGAN ALGORITMA GENETIKA

open access: yesMajalah Ilmiah Teknologi Elektro, 2014
Teknik clustering saat ini telah banyak digunakan untuk mengatasi permasalahan yang terkait dengansegementasi data. Implementasi clustering ini dapat diterapkan pada berbagai bidang sebagai contoh dalam halpemasaran, clustering dapat digunakan sebagai ...
Pivin Suwirmayanti   +2 more
doaj  

STUDI ANALISA PELATIHAN JARINGAN SYARAF TIRUAN DENGAN DAN TANPA ALGORITMA GENETIKA

open access: yesJurnal Informatika, 2002
Neural network as an information processor system which has some similarities with human brain, is lately used to solve general problems. Neural network has several characteristics based on : architecture, learning algorithm, and activation function ...
Agustinus Noertjahyana, Yulia Yulia
doaj  

PENJADUALAN FLOWSHOP DENGAN ALGORITMA GENETIKA

open access: yesJurnal Teknik Industri, 1999
This paper explains and gives an application of genetic algorithm for flowshop scheduling at "X" company to reach minimum multiple objectives of makespan, total flowtime and machine idletime.
Danny Prabowo Soetanto   +1 more
doaj  

Autism and duplication of 17q12q21.2 by array-CGH: a case report. [PDF]

open access: yesRev Paul Pediatr, 2023
Weingartner A   +10 more
europepmc   +1 more source

Genetika talasemija

open access: yes
Thalassemias are a group of inherited hemoglobinopathies caused by impaired synthesis of globin chains, most commonly due to point causal sequence variant or deletions in the genes encoding α- or β-globin. Depending on the affected chain, thalassemias are classified as alpha or beta types, with clinical severity ranging from mild, asymptomatic forms to
openaire   +1 more source

Urinary detection of high-risk HPV DNA to enhance cervical cancer screening in developing countries. [PDF]

open access: yesMicrobiol Spectr
Intan NS   +9 more
europepmc   +1 more source

Genetika autoimunosnih bolesti

open access: yes, 2015
Autoimmune diseases are very complex diseases that keep affecting more and more people. Since they are the result of genetic disorders and enviromental factors, they appear with a large spectrum of symptoms which makes their characterization and discovering their real cause even more difficult.
openaire   +1 more source

Home - About - Disclaimer - Privacy